A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176502



Internal ID15528628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127906678..127954482hg38UCSC Ensembl
Innerchr9:130668957..130716761hg19UCSC Ensembl
Innerchr9:129708778..129756582hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3847805
hg1947805
hg1847805
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615381
Supporting Variants
SamplesHGDP00668
Known GenesDPM2, FAM102A, PIP5KL1, ST6GALNAC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176502
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