A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6523924



Internal ID20897285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33129881..33140213hg38UCSC Ensembl
chr19:33620787..33631119hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3810333
hg1910333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197322
Samples
Known GenesGPATCH1, WDR88
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6523924
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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