A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532629



Internal ID20905990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14694493..14844127hg38UCSC Ensembl
chr19:14805305..14954939hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38149635
hg19149635
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197411
Samples
Known GenesEMR2, OR7A10, OR7A5, OR7C1, ZNF333
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532629
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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