A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6601n100



Internal ID22792688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119926774..119998067hg38UCSC Ensembl
chr7:119566828..119638121hg19UCSC Ensembl
chr7:119354064..119425357hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3871294
hg1971294
hg1871294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030051, nsv1034757, nsv1022301, nsv1033844, nsv1022766, nsv1023232, nsv1030379
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)dgv6601n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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