A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569049



Internal ID21761092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23606365..23606365hg38UCSC Ensembl
chr7:23645984..23645984hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6064737
Supporting Variants
Samples
Known GenesCCDC126
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569049
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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