A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148880



Internal ID15855027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55982245..56032253hg38UCSC Ensembl
Innerchr15:56274443..56324451hg19UCSC Ensembl
Innerchr15:54061735..54111743hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3850009
hg1950009
hg1850009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv569545
Supporting Variants
Samples1780862416_A
Known GenesNEDD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148880
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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