A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502863



Internal ID20876111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19679701..19714800hg38UCSC Ensembl
chr17:19583014..19618113hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3835100
hg1935100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034826
Samples
Known GenesSLC47A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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