A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006122



Internal ID22067753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7829081..7844786hg38UCSC Ensembl
Outerchr9:7826457..7849232hg38UCSC Ensembl
Innerchr9:7829081..7844786hg19UCSC Ensembl
Outerchr9:7826457..7849232hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3822776
hg1922776
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154420
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006122
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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