A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752131



Internal ID12985683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91294585..91391985hg38UCSC Ensembl
Innerchr6:92004303..92101703hg19UCSC Ensembl
Innerchr6:92061024..92158424hg18UCSC Ensembl
Innerchr6:92061024..92158424hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3897401
hg1997401
hg1897401
hg1797401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6982625, essv6989659
SamplesBEC_572
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752131
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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