A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032688



Internal ID18775222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158869559..159327018hg38UCSC Ensembl
Innerchr7:158662250..159119708hg19UCSC Ensembl
Innerchr7:158355011..158812469hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38457460
hg19457459
hg18457459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674787
Samples
Known GenesLINC00689, VIPR2, WDR60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032688
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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