A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099599



Internal ID15606099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152319159..152373073hg38UCSC Ensembl
Innerchr7:152016244..152070158hg19UCSC Ensembl
Innerchr7:151647177..151701091hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3853915
hg1953915
hg1853915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv609050
Supporting Variants
Samples
Known GenesKMT2C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1099599
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