A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099445



Internal ID20666485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178690967..178696395hg38UCSC Ensembl
chr3:178408755..178414183hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg385429
hg195429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371116
Supporting Variants
Samples
Known GenesKCNMB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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