A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176521



Internal ID15877282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133650175..133663599hg38UCSC Ensembl
Innerchr9:136515297..136528721hg19UCSC Ensembl
Innerchr9:135505118..135518542hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3813425
hg1913425
hg1813425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615640
Supporting Variants
SamplesHGDP00961
Known GenesDBH, DBH-AS1, SARDH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176521
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