A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025627



Internal ID19114845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6523056..6648098hg38UCSC Ensembl
Innerchr9:6523056..6648098hg19UCSC Ensembl
Innerchr9:6513056..6638098hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38125043
hg19125043
hg18125043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689082
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)nsv1025627
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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