A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155934



Internal ID15879285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:157809604..157866004hg38UCSC Ensembl
Innerchr7:157602296..157658696hg19UCSC Ensembl
Innerchr7:157295057..157351457hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3856401
hg1956401
hg1856401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609247
Supporting Variants
SamplesHGDP01339
Known GenesLOC100506585, PTPRN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155934
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