A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752236



Internal ID15699506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86756311..86757011hg38UCSC Ensembl
Innerchr10:88516068..88516768hg19UCSC Ensembl
Innerchr10:88506048..88506748hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38701
hg19701
hg18701
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551795
Supporting Variants
Samples
Known GenesBMPR1A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752236
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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