A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501807



Internal ID20875044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42084362..42103755hg38UCSC Ensembl
chr17:40236380..40255773hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3819394
hg1919394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188544
Samples
Known GenesDHX58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501807
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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