A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1173768



Internal ID15506715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:13577220..13590502hg38UCSC Ensembl
Innerchr1:13903715..13916997hg19UCSC Ensembl
Innerchr1:13776302..13789584hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3813283
hg1913283
hg1813283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545568
Supporting Variants
Samples1780854159_A
Known GenesPDPN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1173768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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