A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6140751



Internal ID339944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173421093..173421173hg38UCSC Ensembl
chr4:174342244..174342324hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961040
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6140751
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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