A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177106



Internal ID20744146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133331053..133344786hg38UCSC Ensembl
chr9:136197889..136211641hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3813734
hg1913753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453170
Supporting Variants
Samples
Known GenesMED22, SURF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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