A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989755



Internal ID12975006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:82613288..82692146hg38UCSC Ensembl
Innerchr1:83078971..83157829hg19UCSC Ensembl
Innerchr1:82851559..82930417hg18UCSC Ensembl
Innerchr1:82790992..82869850hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3878859
hg1978859
hg1878859
hg1778859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750841
Supporting Variants
SamplesBEC_557
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989755
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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