A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414264



Internal ID21071817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:78499922..78503716hg38UCSC Ensembl
chr5:77795745..77799539hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg383795
hg193795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133965
Samples
Known GenesLHFPL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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