A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34437



Internal ID12643790
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 StatusM
Merged Variants
Supporting Variantsessv6978801, essv6978800
SamplesNA12264
Known GenesGCNT2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34437
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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