A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5436626



Internal ID215239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6812724..6820716hg38UCSC Ensembl
chr4:6814451..6822443hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg387993
hg197993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16945390
Samples
Known GenesKIAA0232
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5436626
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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