A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020761



Internal ID19109979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109568130..109635643hg38UCSC Ensembl
Innerchr7:109208187..109275700hg19UCSC Ensembl
Innerchr7:108995423..109062936hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3867514
hg1967514
hg1867514
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656232
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)nsv1020761
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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