A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047761



Internal ID19136980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:115693548..115836092hg38UCSC Ensembl
Innerchr9:118455827..118598371hg19UCSC Ensembl
Innerchr9:117495648..117638192hg18UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg38142545
hg19142545
hg18142545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695163
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)nsv1047761
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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