A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532607



Internal ID308526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58046447..58046887hg38UCSC Ensembl
chr19:58557815..58558255hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724409
Samples
Known GenesZSCAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532607
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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