A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982625



Internal ID12975283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91300527..91391985hg38UCSC Ensembl
Innerchr6:92010245..92101703hg19UCSC Ensembl
Innerchr6:92066966..92158424hg18UCSC Ensembl
Innerchr6:92066966..92158424hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3891459
hg1991459
hg1891459
hg1791459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752131
Supporting Variants
SamplesBEC_572
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982625
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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