A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061977



Internal ID18804508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87754432..87775222hg38UCSC Ensembl
Innerchr16:87788038..87808828hg19UCSC Ensembl
Innerchr16:86345539..86366329hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3820791
hg1920791
hg1820791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719121
Samples
Known GenesKLHDC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061977
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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