A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6077249



Internal ID21986482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42883954..42883954hg38UCSC Ensembl
chr7:42923553..42923553hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6077249
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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