A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547626



Internal ID16335035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:120108862..120134055hg38UCSC Ensembl
Innerchr1:120651448..120676626hg19UCSC Ensembl
Innerchr1:120452971..120478149hg18UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg3825194
hg1925179
hg1825179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv723016
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547626
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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