A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6304n100



Internal ID22792391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:19535054..19615001hg38UCSC Ensembl
chr7:19574677..19654624hg19UCSC Ensembl
chr7:19541202..19621149hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3879948
hg1979948
hg1879948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032609, nsv1016344
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)dgv6304n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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