A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437365



Internal ID22495235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141085584..141086145hg38UCSC Ensembl
chr7:140785384..140785945hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919186
Supporting Variants
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437365
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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