A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174732



Internal ID15881028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132348013..132477022hg38UCSC Ensembl
Innerchr10:134161517..134290526hg19UCSC Ensembl
Innerchr10:134011507..134140516hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38129010
hg19129010
hg18129010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552507
Supporting Variants
SamplesNINDS_60
Known GenesC10orf91, LRRC27, PWWP2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174732
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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