A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575901



Internal ID16016624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67393189..67403637hg38UCSC Ensembl
Innerchr17:65389305..65399753hg19UCSC Ensembl
Innerchr17:62819767..62830215hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3810449
hg1910449
hg1810449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5751n54
Supporting Variantsnssv875852
Samples
Known GenesPITPNC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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