A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552023



Internal ID15992746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97355926..97407679hg38UCSC Ensembl
Innerchr10:99115683..99167436hg19UCSC Ensembl
Innerchr10:99105673..99157426hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3851754
hg1951754
hg1851754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1369n54
Supporting Variantsnssv1174567
Samples1780862019_A
Known GenesRRP12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552023
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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