A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545735



Internal ID15986458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21215242..21221575hg38UCSC Ensembl
Innerchr1:21541735..21548068hg19UCSC Ensembl
Innerchr1:21414322..21420655hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg386334
hg196334
hg186334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv711288
Samples
Known GenesECE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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