A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017565



Internal ID18760099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152450845..152758187hg38UCSC Ensembl
Innerchr7:152147930..152455272hg19UCSC Ensembl
Innerchr7:151778863..152086205hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38307343
hg19307343
hg18307343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674275
Samples
Known GenesLINC01003, XRCC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017565
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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