A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037964



Internal ID19127183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:130808049..130821552hg38UCSC Ensembl
Innerchr9:133683436..133696939hg19UCSC Ensembl
Innerchr9:132673257..132686760hg18UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg3813504
hg1913504
hg1813504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695284
Samples
Known GenesABL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037964
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer