A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516429



Internal ID15443722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:176166387..176240071hg38UCSC Ensembl
Innerchr3:175884175..175957859hg19UCSC Ensembl
Innerchr3:177366869..177440553hg18UCSC Ensembl
Innerchr3:177366877..177440561hg17UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3873685
hg1973685
hg1873685
hg1773685
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687669, nssv690632, nssv661073, nssv676810, nssv669136, nssv671829, nssv679025, nssv672966, nssv692520, nssv676962, nssv679362, nssv660692, nssv675733, nssv678399, nssv691459, nssv692191, nssv691557, nssv681784, nssv671130, nssv654135, nssv694019, nssv661303, nssv678124, nssv673128, nssv660018, nssv659145, nssv666157, nssv663414, nssv659615, nssv689612, nssv658741, nssv681309, nssv661568, nssv673363, nssv681381, nssv660357, nssv667688, nssv656309, nssv684508, nssv691795, nssv685299, nssv687009, nssv671093, nssv672533, nssv663265, nssv652694, nssv656616, nssv672680, nssv667773, nssv687115, nssv668435, nssv686467, nssv676612, nssv655287, nssv660290, nssv681045, nssv673110, nssv669037, nssv652909, nssv658258, nssv677408
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516429
Frequency
Sample Size2026
Observed Gain13
Observed Loss48
Observed Complex0
Frequencyn/a


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