A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3666977



Internal ID18618572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12813166..12971126hg38UCSC Ensembl
Innerchr8:12670675..12828635hg19UCSC Ensembl
Innerchr8:12715046..12873006hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38157961
hg19157961
hg18157961
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033835
Supporting Variants
Samples
Known GenesKIAA1456, LINC00681
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3666977
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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