A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv760499



Internal ID16054455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127179990..127190882hg38UCSC Ensembl
Innerchr10:128978254..128989146hg19UCSC Ensembl
Innerchr10:128868244..128879136hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3810893
hg1910893
hg1810893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552300
Supporting Variants
Samples
Known GenesDOCK1, FAM196A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv760499
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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