A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980317



Internal ID12631498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38271459..38347159hg38UCSC Ensembl
Innerchr7:38311060..38386760hg19UCSC Ensembl
Innerchr7:38277585..38353285hg18UCSC Ensembl
Innerchr7:38084300..38160000hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3875701
hg1975701
hg1875701
hg1775701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34699
Supporting Variants
SamplesNA07034
Known GenesTARP, TRG-AS1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980317
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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