A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6322n100



Internal ID20157938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38240623..38286323hg38UCSC Ensembl
chr7:38280224..38325924hg19UCSC Ensembl
chr7:38246749..38292449hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3845701
hg1945701
hg1845701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1026846, nsv1030933
Samples
Known GenesTARP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6322n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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