A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551586



Internal ID16338995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79376259..79418622hg38UCSC Ensembl
Innerchr10:81136015..81178378hg19UCSC Ensembl
Innerchr10:80806021..80848384hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3842364
hg1942364
hg1842364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1279n54
Supporting Variantsnssv1174549
SamplesNINDS_49
Known GenesZCCHC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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