A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018870



Internal ID19108087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6548393..6708345hg38UCSC Ensembl
Innerchr9:6548393..6708345hg19UCSC Ensembl
Innerchr9:6538393..6698345hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38159953
hg19159953
hg18159953
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7389n100
Supporting Variantsnssv3758103
Samples
Known GenesGLDC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018870
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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