A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751763



Internal ID15699033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79242663..79243323hg38UCSC Ensembl
Innerchr10:81002420..81003080hg19UCSC Ensembl
Innerchr10:80672426..80673086hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38661
hg19661
hg18661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551580
Supporting Variants
Samples
Known GenesZMIZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751763
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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