A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6383n100



Internal ID22792470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:61081237..62335035hg38UCSC Ensembl
chr7:61063962..61779286hg19UCSC Ensembl
chr7:61067904..61416721hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg381253799
hg19715325
hg18348818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018596, nsv1021890
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)dgv6383n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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