A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559961



Internal ID18511556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84750052..85139204hg38UCSC Ensembl
Innerchr16:84783658..85172810hg19UCSC Ensembl
Innerchr16:83341159..83730311hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38389153
hg19389153
hg18389153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066260
Supporting Variants
Samples
Known GenesCRISPLD2, FAM92B, KIAA0513, LOC400548, USP10, ZDHHC7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559961
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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