A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371635



Internal ID21029188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20756901..20763200hg38UCSC Ensembl
chr4:20758524..20764823hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113274
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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