A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009498



Internal ID21918841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136973053..136973209hg38UCSC Ensembl
chr7:136657800..136657956hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17573611
Samples
Known GenesCHRM2, LOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009498
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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