A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425529



Internal ID204491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35106379..35107212hg38UCSC Ensembl
chr1:35571980..35572813hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902011
Samples
Known GenesZMYM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425529
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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