A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517045



Internal ID20890406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56554518..56555126hg38UCSC Ensembl
chr19:57065887..57066495hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049338
Samples
Known GenesZFP28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517045
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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