A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545626



Internal ID15986349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15827072..15834894hg38UCSC Ensembl
Innerchr1:16153567..16161389hg19UCSC Ensembl
Innerchr1:16026154..16033976hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg387823
hg197823
hg187823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv154n54
Supporting Variantsnssv710805
Samples
Known GenesFLJ37453
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545626
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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