A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047919



Internal ID18790450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112407026..112446554hg38UCSC Ensembl
Innerchr9:115169306..115208834hg19UCSC Ensembl
Innerchr9:114209127..114248655hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3839529
hg1939529
hg1839529
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695053
Samples
Known GenesHSDL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047919
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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