A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987763



Internal ID12631505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38279738..38347190hg38UCSC Ensembl
Innerchr7:38319339..38386791hg19UCSC Ensembl
Innerchr7:38285864..38353316hg18UCSC Ensembl
Innerchr7:38092579..38160031hg17UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3867453
hg1967453
hg1867453
hg1767453
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34699
Supporting Variants
SamplesNA07034
Known GenesTRG-AS1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987763
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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