A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516166



Internal ID15096773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:34849610..34880179hg38UCSC Ensembl
Innerchr7:34889222..34919791hg19UCSC Ensembl
Innerchr7:34855747..34886316hg18UCSC Ensembl
Innerchr7:34662462..34693031hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3830570
hg1930570
hg1830570
hg1730570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv418n21
Supporting Variantsnssv675101, nssv684446, nssv671454, nssv680782, nssv658081, nssv669260, nssv683249, nssv687420, nssv655741, nssv687185, nssv675915, nssv675891, nssv689007, nssv677882, nssv689319, nssv658464, nssv666837, nssv689594, nssv666571, nssv672994, nssv681092, nssv658731
Samples
Known GenesNPSR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516166
Frequency
Sample Size2026
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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