A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545689



Internal ID15986412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16921023..16936882hg38UCSC Ensembl
Innerchr1:17247518..17263377hg19UCSC Ensembl
Innerchr1:17120105..17135964hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3815860
hg1915860
hg1815860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171n54
Supporting Variantsnssv710922
Samples
Known GenesCROCC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545689
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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