A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016077



Internal ID19105295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11459329..11623397hg38UCSC Ensembl
Innerchr9:11459329..11623397hg19UCSC Ensembl
Innerchr9:11449329..11613397hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38164069
hg19164069
hg18164069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7411n100
Supporting Variantsnssv3758170
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)nsv1016077
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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