A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436582



Internal ID22494452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139140004..139146980hg38UCSC Ensembl
chr7:138824750..138831726hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg386977
hg196977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925443
Supporting Variants
Samples
Known GenesTTC26
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436582
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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