A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064677



Internal ID18807208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84384525..84462657hg38UCSC Ensembl
Innerchr16:84418131..84496263hg19UCSC Ensembl
Innerchr16:82975632..83053764hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3878133
hg1978133
hg1878133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559949
Samples
Known GenesATP2C2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064677
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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