A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053964



Internal ID20621004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173079869..173194468hg38UCSC Ensembl
chr1:173049009..173163607hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38114600
hg19114599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6333541
Supporting Variants
Samples
Known GenesTNFSF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053964
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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