A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156497



Internal ID20723537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38252701..38362800hg38UCSC Ensembl
chr7:38292302..38402401hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38110100
hg19110100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608338
Supporting Variants
Samples
Known GenesTARP, TRG-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156497
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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