A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364813



Internal ID21022366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17894101..17897000hg38UCSC Ensembl
chr4:17895724..17898623hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113816
Samples
Known GenesLCORL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364813
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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