A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6339n100



Internal ID22792426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40398879..40449484hg38UCSC Ensembl
chr7:40438478..40489083hg19UCSC Ensembl
chr7:40405003..40455608hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3850606
hg1950606
hg1850606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032883, nsv1026022, nsv1027075, nsv1019992, nsv1032028
Samples
Known GenesC7orf10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6339n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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