A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155135



Internal ID20722175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137303556..137304009hg38UCSC Ensembl
chr7:136988303..136988756hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418642
Supporting Variants
Samples
Known GenesPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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