A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990486



Internal ID12635812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:2650601..3089361hg38UCSC Ensembl
Innerchr10:2692793..3131553hg19UCSC Ensembl
Innerchr10:2682793..3121553hg18UCSC Ensembl
Innerchr10:2682793..3121553hg17UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38438761
hg19438761
hg18438761
hg17438761
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34832
Supporting Variants
SamplesNA19201
Known GenesPFKP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990486
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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