A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061134



Internal ID21970367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117864742..117864742hg38UCSC Ensembl
chr7:117504796..117504796hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575708
Samples
Known GenesCTTNBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061134
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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