A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18120064



Internal ID20687104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71186101..71187500hg38UCSC Ensembl
chr4:72051818..72053217hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6386299
Supporting Variants
Samples
Known GenesSLC4A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18120064
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07121


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