A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176156



Internal ID15530703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135698292..135752357hg38UCSC Ensembl
Innerchr9:138590138..138644203hg19UCSC Ensembl
Innerchr9:137729959..137784024hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3854066
hg1954066
hg1854066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615922
Supporting Variants
SamplesHGDP00977
Known GenesKCNT1, SOHLH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176156
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