A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980185



Internal ID12981405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74346526..74421020hg38UCSC Ensembl
Innerchr6:75056242..75130736hg19UCSC Ensembl
Innerchr6:75112962..75187456hg18UCSC Ensembl
Innerchr6:75112962..75187456hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3874495
hg1974495
hg1874495
hg1774495
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980185
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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