A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559952



Internal ID18511547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84401623..84438300hg38UCSC Ensembl
Innerchr16:84435229..84471906hg19UCSC Ensembl
Innerchr16:82992730..83029407hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3836678
hg1936678
hg1836678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066356
Supporting Variants
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)nssv3559952
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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