A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18115947



Internal ID20682987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37277101..37279600hg38UCSC Ensembl
chr4:37278723..37281222hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6393494
Supporting Variants
Samples
Known GenesKIAA1239
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18115947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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