A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509976



Internal ID20883289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43783801..43795600hg38UCSC Ensembl
chr17:41861169..41872968hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3811800
hg1911800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196050
Samples
Known GenesC17orf105
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509976
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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