A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121016



Internal ID20688056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74957971..74959475hg38UCSC Ensembl
chr4:75883181..75884685hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381505
hg191505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385280
Supporting Variants
Samples
Known GenesPARM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121016
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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