A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001636



Internal ID21910979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98863211..98863729hg38UCSC Ensembl
chr7:98460834..98461352hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561462
Samples
Known GenesTMEM130
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001636
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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