A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027565



Internal ID19116784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136854535hg38UCSC Ensembl
Innerchr8:137687873..137866778hg19UCSC Ensembl
Innerchr8:137757055..137935960hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38178906
hg19178906
hg18178906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3690031
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027565
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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