A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6444n100



Internal ID22792531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65587265..65874892hg38UCSC Ensembl
chr7:65052178..65339879hg19UCSC Ensembl
chr7:64689613..64977314hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38287628
hg19287702
hg18287702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033400, nsv1025207
Samples
Known GenesCCT6P1, INTS4L2, LOC441242, SNORA22, VKORC1L1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6444n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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