A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015928



Internal ID21925271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148394302..148397130hg38UCSC Ensembl
chr7:148091394..148094222hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg382829
hg192829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577254
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015928
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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