A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6434n100



Internal ID22792521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64060367..64341728hg38UCSC Ensembl
chr7:63520745..63802106hg19UCSC Ensembl
chr7:63158180..63439541hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38281362
hg19281362
hg18281362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019217, nsv1027639
Samples
Known GenesZNF679, ZNF727, ZNF735, ZNF736
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6434n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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