A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978800



Internal ID12632450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10456877..10540980hg38UCSC Ensembl
Innerchr6:10457110..10541213hg19UCSC Ensembl
Innerchr6:10565096..10649199hg18UCSC Ensembl
Innerchr6:10565096..10649199hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3884104
hg1984104
hg1884104
hg1784104
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34437
Supporting Variants
SamplesNA12264
Known GenesGCNT2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978800
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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