A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980186



Internal ID12981406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74348473..74402999hg38UCSC Ensembl
Innerchr6:75058189..75112715hg19UCSC Ensembl
Innerchr6:75114909..75169435hg18UCSC Ensembl
Innerchr6:75114909..75169435hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3854527
hg1954527
hg1854527
hg1754527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35015
Supporting Variants
SamplesNA18967
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980186
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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