A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504067



Internal ID20877326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35785984..35797861hg38UCSC Ensembl
chr17:34112988..34124865hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3811878
hg1911878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193900
Samples
Known GenesMMP28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504067
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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