A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518572



Internal ID20891933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51033409..51036120hg38UCSC Ensembl
chr19:51536665..51539377hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg382712
hg192713
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048702
Samples
Known GenesKLK12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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