A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022278



Internal ID19111496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13301945..13340591hg38UCSC Ensembl
Innerchr9:13301944..13340590hg19UCSC Ensembl
Innerchr9:13291944..13330590hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3838647
hg1938647
hg1838647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7458n100
Supporting Variantsnssv3690603
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)nsv1022278
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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