A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020826



Internal ID19110044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42729314..42856259hg38UCSC Ensembl
Innerchr9:44114860..44241805hg19UCSC Ensembl
Innerchr9:44054856..44181801hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38126946
hg19126946
hg18126946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7573n100
Supporting Variantsnssv3693002, nssv3693000, nssv3693001, nssv3693003
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)nsv1020826
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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