A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6617n100



Internal ID20158233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131331684..131555085hg38UCSC Ensembl
chr7:131016443..131239844hg19UCSC Ensembl
chr7:130666983..130890384hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38223402
hg19223402
hg18223402
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029950, nsv1027676
Samples
Known GenesMKLN1, PODXL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6617n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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