A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517570



Internal ID20890931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6172163..6178039hg38UCSC Ensembl
chr19:6172174..6178050hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385877
hg195877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049953
Samples
Known GenesACSBG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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