A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176432



Internal ID20743472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137598212..137601984hg38UCSC Ensembl
chr9:140492664..140496436hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg383773
hg193773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448857
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176432
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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