A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532127



Internal ID20905488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63843490..63844884hg38UCSC Ensembl
chr17:61920850..61922244hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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