A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv748834



Internal ID16042790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57707602..57797870hg38UCSC Ensembl
Innerchr10:59467362..59557630hg19UCSC Ensembl
Innerchr10:59137368..59227636hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3890269
hg1990269
hg1890269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551147
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv748834
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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