A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512276



Internal ID20885608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:11043481..11048891hg38UCSC Ensembl
chr17:10946798..10952208hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385411
hg195411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034066
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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