A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189995



Internal ID20757035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88792519..88814442hg38UCSC Ensembl
chr9:91407434..91429357hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3821924
hg1921924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440538
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189995
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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