A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027596



Internal ID19116815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26265536..26425834hg38UCSC Ensembl
Innerchr9:26265534..26425832hg19UCSC Ensembl
Innerchr9:26255534..26415832hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38160299
hg19160299
hg18160299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7484n100
Supporting Variantsnssv3691992, nssv3691989, nssv3691994, nssv3755874, nssv3691990, nssv3755875, nssv3691993, nssv3755876, nssv3691991, nssv3755873
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027596
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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