A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050000



Internal ID18792531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31078208..31104430hg38UCSC Ensembl
Innerchr15:31370411..31396633hg19UCSC Ensembl
Innerchr15:29157703..29183925hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3826223
hg1926223
hg1826223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3547656, nssv3547655
Samples
Known GenesTRPM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050000
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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