A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556925



Internal ID15997648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:758338..763878hg38UCSC Ensembl
Innerchr12:867504..873044hg19UCSC Ensembl
Innerchr12:737765..743305hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg385541
hg195541
hg185541
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2259n54
Supporting Variantsnssv786096, nssv786097
Samples
Known GenesWNK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556925
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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