A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1100358



Internal ID15953544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156219536..156232702hg38UCSC Ensembl
Innerchr7:156012230..156025396hg19UCSC Ensembl
Innerchr7:155704991..155718157hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3813167
hg1913167
hg1813167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609169
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1100358
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