A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552506



Internal ID16339915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:132345217..132470371hg38UCSC Ensembl
Innerchr10:134158721..134283875hg19UCSC Ensembl
Innerchr10:134008711..134133865hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38125155
hg19125155
hg18125155
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1458n54
Supporting Variantsnssv1174731
SamplesNINDS_50
Known GenesC10orf91, LRRC27, PWWP2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552506
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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