A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155243



Internal ID20722283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139134140..139136017hg38UCSC Ensembl
chr7:138818886..138820763hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381878
hg191878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420078
Supporting Variants
Samples
Known GenesTTC26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155243
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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