A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508236



Internal ID20881535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43183052..43187426hg38UCSC Ensembl
chr17:41335069..41339443hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg384375
hg194375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035691
Samples
Known GenesNBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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