A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6329n100



Internal ID20157945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38271110..38312626hg38UCSC Ensembl
chr7:38310711..38352227hg19UCSC Ensembl
chr7:38277236..38318752hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3841517
hg1941517
hg1841517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030077, nsv1018379, nsv1033991, nsv1029931
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)dgv6329n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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