A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000823



Internal ID6712965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:38232022..38350519hg38UCSC Ensembl
Outerchr7:38271623..38390120hg19UCSC Ensembl
Outerchr7:38238148..38356645hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38118498
hg19118498
hg18118498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564960
SamplesHuRef
Known GenesTARP, TRG-AS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000823
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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