A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986636



Internal ID12635389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:59096142..59179302hg38UCSC Ensembl
Innerchr10:60855902..60939062hg19UCSC Ensembl
Innerchr10:60525908..60609068hg18UCSC Ensembl
Innerchr10:60525908..60609068hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3883161
hg1983161
hg1883161
hg1783161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34715
Supporting Variants
SamplesNA19127
Known GenesPHYHIPL
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986636
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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