A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148344



Internal ID16001530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136975638..136980181hg38UCSC Ensembl
Innerchr9:139870090..139874633hg19UCSC Ensembl
Innerchr9:138989911..138994454hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg384544
hg194544
hg184544
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615992
Supporting Variants
Samples
Known GenesPTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148344
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