A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532634



Internal ID20905995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16166226..16167156hg38UCSC Ensembl
chr19:16277037..16277967hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044469
Samples
Known GenesCIB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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