A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515217



Internal ID20888576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7595191..7595744hg38UCSC Ensembl
chr17:7498509..7499062hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196352
Samples
Known GenesFXR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515217
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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