A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155926



Internal ID15877775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155174824..155187164hg38UCSC Ensembl
Innerchr7:154966534..154978874hg19UCSC Ensembl
Innerchr7:154597467..154609807hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3812341
hg1912341
hg1812341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609119
Supporting Variants
SamplesHGDP01044
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155926
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