A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065925



Internal ID20632965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9872471..9877579hg38UCSC Ensembl
chr1:9932529..9937637hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg385109
hg195109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319709
Supporting Variants
Samples
Known GenesCTNNBIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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