A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv796061



Internal ID16090017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52692747..52693422hg38UCSC Ensembl
Innerchr12:53086531..53087206hg19UCSC Ensembl
Innerchr12:51372798..51373473hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38676
hg19676
hg18676
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558946
Supporting Variants
Samples
Known GenesKRT77
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv796061
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer