A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498734



Internal ID20871947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1756201..1762000hg38UCSC Ensembl
chr17:1659495..1665294hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg385800
hg195800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180602
Samples
Known GenesSERPINF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498734
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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