A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15704291



Internal ID21376567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141167519..141167741hg38UCSC Ensembl
chr7:140867319..140867541hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4388700
Supporting Variants
Samples
Known GenesTMEM178B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nssv15704291
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00574713


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