A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066581



Internal ID21975814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140171518..140171518hg38UCSC Ensembl
chr7:139871318..139871318hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570225
Samples
Known GenesKDM7A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066581
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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