A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18038998



Internal ID20606038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7728594..7735459hg38UCSC Ensembl
chr17:7631912..7638777hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg386866
hg196866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498582
Supporting Variants
Samples
Known GenesDNAH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18038998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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