A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532484



Internal ID20905845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57749401..57750000hg38UCSC Ensembl
chr19:58260769..58261368hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049496
Samples
Known GenesZNF776
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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