A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076286



Internal ID21985519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74025572..74025572hg38UCSC Ensembl
chr7:73439902..73439902hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17574357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076286
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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