A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032232



Internal ID19121454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169183816..170049076hg38UCSC Ensembl
Innerchr6:169583911..170364300hg19UCSC Ensembl
Innerchr6:169325836..170206225hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38865261
hg19780390
hg18880390
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3653084
Samples
Known GenesC6orf120, ERMARD, LINC00242, LINC00574, PHF10, TCTE3, THBS2, WDR27
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032232
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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