A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031673



Internal ID19120895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:1018373..1427973hg38UCSC Ensembl
Innerchr8:968373..1376139hg19UCSC Ensembl
Innerchr8:955780..1363546hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38409601
hg19407767
hg18407767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3675031
Samples
Known GenesERICH1-AS1, LOC286083
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031673
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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