A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv761972



Internal ID16055928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132731265..132737378hg38UCSC Ensembl
Innerchr10:134544769..134550882hg19UCSC Ensembl
Innerchr10:134394759..134400872hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386114
hg196114
hg186114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552527
Supporting Variants
Samples
Known GenesINPP5A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv761972
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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