A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150116



Internal ID20717156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123935191..123935563hg38UCSC Ensembl
chr7:123575245..123575617hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602982
Supporting Variants
Samples
Known GenesSPAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150116
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00084


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