A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517688



Internal ID15444981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:161232901..161237770hg38UCSC Ensembl
Innerchr4:162154053..162158922hg19UCSC Ensembl
Innerchr4:162373503..162378372hg18UCSC Ensembl
Innerchr4:162511658..162516527hg17UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg384870
hg194870
hg184870
hg174870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685949, nssv669018, nssv652843, nssv661389
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517688
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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