A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191271



Internal ID20758311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96087887..96088894hg38UCSC Ensembl
chr9:98850169..98851176hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg381008
hg191008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448829
Supporting Variants
Samples
Known GenesLOC158435
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191271
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00159


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