A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685354



Internal ID18636949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:21917803..21972691hg38UCSC Ensembl
Innerchr8:21775314..21830202hg19UCSC Ensembl
Innerchr8:21831260..21886148hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3854889
hg1954889
hg1854889
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017189
Supporting Variants
Samples
Known GenesXPO7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685354
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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