A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18107570



Internal ID20674611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103403669..103404166hg38UCSC Ensembl
chr4:104324826..104325323hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394868
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18107570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00049


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