A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066260



Internal ID18808791
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 StatusM
Merged Variants
Supporting Variantsnssv3559961
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)nsv1066260
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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