A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153137



Internal ID20720177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144692110..144705302hg38UCSC Ensembl
chr7:144389203..144402395hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3813193
hg1913193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427597
Supporting Variants
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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