A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551591



Internal ID16339000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79445023..79445987hg38UCSC Ensembl
Innerchr10:81204779..81205743hg19UCSC Ensembl
Innerchr10:80874785..80875749hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38965
hg19965
hg18965
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv751774
Samples
Known GenesZCCHC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551591
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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