A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978801



Internal ID12632444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10471029..10502777hg38UCSC Ensembl
Innerchr6:10471262..10503010hg19UCSC Ensembl
Innerchr6:10579248..10610996hg18UCSC Ensembl
Innerchr6:10579248..10610996hg17UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg3831749
hg1931749
hg1831749
hg1731749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34437
Supporting Variants
SamplesNA12264
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978801
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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