A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429647



Internal ID208488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35391816..35391914hg38UCSC Ensembl
chr1:35857417..35857515hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903676
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429647
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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