A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550144



Internal ID16337553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:20162679..20207341hg38UCSC Ensembl
Innerchr10:20451608..20496270hg19UCSC Ensembl
Innerchr10:20491614..20536276hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3844663
hg1944663
hg1844663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv989n54
Supporting Variantsnssv1174146
SamplesNINDS_183
Known GenesPLXDC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550144
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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