A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027629



Internal ID19116848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26034118..26069180hg38UCSC Ensembl
Innerchr9:26034116..26069178hg19UCSC Ensembl
Innerchr9:26024116..26059178hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg3835063
hg1935063
hg1835063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691987
Samples
Known GenesLOC100506422
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027629
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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