A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055626



Internal ID18798157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87736098..87825570hg38UCSC Ensembl
Innerchr16:87769704..87859176hg19UCSC Ensembl
Innerchr16:86327205..86416677hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3889473
hg1989473
hg1889473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3062n100
Supporting Variantsnssv3719120
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)nsv1055626
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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