A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509089



Internal ID20882395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:1765022..1773349hg38UCSC Ensembl
chr17:1668316..1676643hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg388328
hg198328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034665
Samples
Known GenesSERPINF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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