A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045648



Internal ID21954912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:204195676..204195676hg38UCSC Ensembl
chr1:204164804..204164804hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531277
Samples
Known GenesKISS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045648
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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