A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6349n100



Internal ID22792436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52851725..52921859hg38UCSC Ensembl
chr7:52919418..52989552hg19UCSC Ensembl
chr7:52886912..52957046hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3870135
hg1970135
hg1870135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1020427, nsv1017323
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)dgv6349n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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