A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499487



Internal ID20872707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8390066..8397372hg38UCSC Ensembl
chr17:8293384..8300690hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387307
hg197307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038817
Samples
Known GenesRNF222
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499487
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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