A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551508



Internal ID15992231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71863519..71905893hg38UCSC Ensembl
Innerchr10:73623277..73665651hg19UCSC Ensembl
Innerchr10:73293283..73335657hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3842375
hg1942375
hg1842375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174254
SamplesHGDP00662
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551508
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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