A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070671



Internal ID21979904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132698175..132698175hg38UCSC Ensembl
chr7:132382934..132382934hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563333
Samples
Known GenesFLJ40288
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070671
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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