A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375662



Internal ID21033215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112297836..112299361hg38UCSC Ensembl
chr4:113218992..113220517hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg381526
hg191526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105619
Samples
Known GenesALPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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