A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527576



Internal ID20900937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4977175..4989625hg38UCSC Ensembl
chr19:4977186..4989636hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812451
hg1912451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049046
Samples
Known GenesKDM4B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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