A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1137200



Internal ID15643700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72406935..72532633hg38UCSC Ensembl
Innerchr9:75021851..75147549hg19UCSC Ensembl
Innerchr9:74211671..74337369hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38125699
hg19125699
hg18125699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614611
Supporting Variants
Samples
Known GenesTMC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1137200
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