A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020855



Internal ID19110073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17929046..17975793hg38UCSC Ensembl
Innerchr9:17929044..17975791hg19UCSC Ensembl
Innerchr9:17919044..17965791hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3846748
hg1946748
hg1846748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690672
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)nsv1020855
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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