A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044932



Internal ID20611972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10572401..10573000hg38UCSC Ensembl
chr19:10683077..10683676hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528360
Supporting Variants
Samples
Known GenesAP1M2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044932
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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