A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18049273



Internal ID20616313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56146801..56147300hg38UCSC Ensembl
chr19:56658170..56658669hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531027
Supporting Variants
Samples
Known GenesZNF444
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18049273
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0218


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