A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045935



Internal ID19135154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73375705..73544030hg38UCSC Ensembl
Innerchr9:75990621..76158946hg19UCSC Ensembl
Innerchr9:75180441..75348766hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38168326
hg19168326
hg18168326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3759768
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)nsv1045935
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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