A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034426



Internal ID19123648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119944097..120015437hg38UCSC Ensembl
Innerchr7:119584151..119655491hg19UCSC Ensembl
Innerchr7:119371387..119442727hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3871341
hg1971341
hg1871341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751525
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)nsv1034426
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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