A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532645



Internal ID20906006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7768415..7825056hg38UCSC Ensembl
chr19:7833301..7889942hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3856642
hg1956642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199038
Samples
Known GenesCLEC4GP1, CLEC4M
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532645
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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