A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034936



Internal ID19124156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6575976..6708345hg38UCSC Ensembl
Innerchr9:6575976..6708345hg19UCSC Ensembl
Innerchr9:6565976..6698345hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38132370
hg19132370
hg18132370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7389n100
Supporting Variantsnssv3758105
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)nsv1034936
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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