A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522816



Internal ID20896177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19394698..19398455hg38UCSC Ensembl
chr19:19505507..19509264hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383758
hg193758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045994
Samples
Known GenesGATAD2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522816
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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