A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562645



Internal ID335591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35292282..35292333hg38UCSC Ensembl
chr1:35757883..35757934hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16900605
Samples
Known GenesZMYM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562645
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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