A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148364



Internal ID16001550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:137191539..137198736hg38UCSC Ensembl
Innerchr9:140085991..140093188hg19UCSC Ensembl
Innerchr9:139205812..139213009hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg387198
hg197198
hg187198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv616010
Supporting Variants
Samples
Known GenesTPRN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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