A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502613



Internal ID20875859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8259414..8261333hg38UCSC Ensembl
chr17:8162732..8164651hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381920
hg191920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038319
Samples
Known GenesPFAS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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