A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532486



Internal ID20905847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56077301..56090400hg38UCSC Ensembl
chr17:54154662..54167761hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3813100
hg1913100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036967
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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