A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378165



Internal ID21035718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:127716581..127717250hg38UCSC Ensembl
chr4:128637736..128638405hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18110473
Samples
Known GenesINTU
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378165
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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