A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978899



Internal ID12632617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29903859..29940184hg38UCSC Ensembl
Innerchr6:29871636..29907961hg19UCSC Ensembl
Innerchr6:29979615..30015940hg18UCSC Ensembl
Innerchr6:29979615..30015940hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3836326
hg1936326
hg1836326
hg1736326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34603
Supporting Variants
SamplesNA12760
Known GenesHCG4B
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978899
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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