A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990022



Internal ID12636812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20312261..20487861hg38UCSC Ensembl
Innerchr13:20886400..21062000hg19UCSC Ensembl
Innerchr13:19784400..19960000hg18UCSC Ensembl
Innerchr13:19784400..19960000hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38175601
hg19175601
hg18175601
hg17175601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751132
Supporting Variants
SamplesSPC_179
Known GenesCRYL1, MIR4499
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990022
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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