A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524405



Internal ID20897766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16197701..16198700hg38UCSC Ensembl
chr19:16308512..16309511hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044472
Samples
Known GenesAP1M1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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