A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34699



Internal ID12644049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38271459..38347190hg38UCSC Ensembl
Innerchr7:38311060..38386791hg19UCSC Ensembl
Innerchr7:38277585..38353316hg18UCSC Ensembl
Innerchr7:38084300..38160031hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3875732
hg1975732
hg1875732
hg1775732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6980317, essv6987763
SamplesNA07034
Known GenesTARP, TRG-AS1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34699
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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