A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056427



Internal ID19145646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75933885..76005861hg38UCSC Ensembl
Innerchr16:75967783..76039759hg19UCSC Ensembl
Innerchr16:74525284..74597260hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3871977
hg1971977
hg1871977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3022n100
Supporting Variantsnssv3559636
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056427
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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