A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097237



Internal ID20664277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174067068..174077953hg38UCSC Ensembl
chr3:173784858..173795743hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3810886
hg1910886
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372245
Supporting Variants
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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