A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149699



Internal ID15854782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13093638..13120279hg38UCSC Ensembl
Innerchr17:12996955..13023596hg19UCSC Ensembl
Innerchr17:12937680..12964321hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3826642
hg1926642
hg1826642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574371
Supporting Variants
Samples1780862312_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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