A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373232



Internal ID21030785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21913050..21915181hg38UCSC Ensembl
chr4:21914673..21916804hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382132
hg192132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18116122
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373232
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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