A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590075



Internal ID16377484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37936223..37945349hg38UCSC Ensembl
Innerchr3:37977714..37986840hg19UCSC Ensembl
Innerchr3:37952718..37961844hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg389127
hg199127
hg189127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8282n54
Supporting Variantsnssv962168, nssv962175, nssv962164, nssv962171, nssv962172, nssv962165, nssv962170, nssv962173, nssv962166, nssv962169, nssv962167, nssv962174
Samples
Known GenesCTDSPL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590075
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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