A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042718



Internal ID19131937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114673026..114726689hg38UCSC Ensembl
Innerchr9:117435306..117488969hg19UCSC Ensembl
Innerchr9:116475127..116528790hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3853664
hg1953664
hg1853664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3695160
Samples
Known GenesLOC100505478
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042718
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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