A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582558



Internal ID16369967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:103057700..103165872hg38UCSC Ensembl
Innerchr2:103674158..103782330hg19UCSC Ensembl
Innerchr2:103040590..103148762hg18UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg38108173
hg19108173
hg18108173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv914703
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582558
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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