A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150736



Internal ID20717776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141080410..141082156hg38UCSC Ensembl
chr7:140780210..140781956hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381747
hg191747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425551
Supporting Variants
Samples
Known GenesTMEM178B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150736
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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