A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073707



Internal ID21982940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:127494930..127494930hg38UCSC Ensembl
chr7:127134984..127134984hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575074
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073707
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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