A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525632



Internal ID20898993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42006967..42007269hg38UCSC Ensembl
chr19:42511119..42511421hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197427
Samples
Known GenesGRIK5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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