A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6403n100



Internal ID22792490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:62367895..62993463hg38UCSC Ensembl
chr7:61812146..62453841hg19UCSC Ensembl
chr7:61449581..62091276hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38625569
hg19641696
hg18641696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025033, nsv1023900, nsv1029383, nsv1025087, nsv1025711, nsv1016125, nsv1031217, nsv1023088, nsv1017346, nsv1015882, nsv1018668, nsv1030517, nsv1035060, nsv1024898, nsv1016794, nsv1033346, nsv1024595, nsv1017338, nsv1022245, nsv1030472
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)dgv6403n100
Frequency
Sample Size11257
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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