A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181637



Internal ID20748677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74877243..74883973hg38UCSC Ensembl
chr9:77492159..77498889hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg386731
hg196731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439528
Supporting Variants
Samples
Known GenesTRPM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181637
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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