A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531102



Internal ID20904463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62806861..62819915hg38UCSC Ensembl
chr17:60884222..60897276hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3813055
hg1913055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190877
Samples
Known GenesMARCH10, MIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531102
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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