A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751996



Internal ID15699266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82136504..82268652hg38UCSC Ensembl
Innerchr10:83896260..84028408hg19UCSC Ensembl
Innerchr10:83886240..84018388hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38132149
hg19132149
hg18132149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551704
Supporting Variants
Samples
Known GenesNRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751996
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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