A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570154



Internal ID21762197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136972934..136973034hg38UCSC Ensembl
chr7:136657681..136657781hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007430
Supporting Variants
Samples
Known GenesCHRM2, LOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570154
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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