A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497741



Internal ID20870949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20213215..20259801hg38UCSC Ensembl
chr17:20116528..20163114hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3846587
hg1946587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034245
Samples
Known GenesSPECC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497741
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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