A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021305



Internal ID19110522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:19256055..19313489hg38UCSC Ensembl
Innerchr7:19295678..19353112hg19UCSC Ensembl
Innerchr7:19262203..19319637hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3857435
hg1957435
hg1857435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643251
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)nsv1021305
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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