A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18109824



Internal ID20676864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:124676101..124677500hg38UCSC Ensembl
chr4:125597256..125598655hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389338
Supporting Variants
Samples
Known GenesANKRD50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18109824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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