A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361673



Internal ID21019226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22446801..22447900hg38UCSC Ensembl
chr4:22448424..22449523hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114580
Samples
Known GenesGPR125
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361673
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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