A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756249



Internal ID16050205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105852798..105922177hg38UCSC Ensembl
Innerchr10:107612556..107681935hg19UCSC Ensembl
Innerchr10:107602546..107671925hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3869380
hg1969380
hg1869380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552100
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)nssv756249
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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