A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6049004



Internal ID21958237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:68636195..68636195hg38UCSC Ensembl
chr1:69101878..69101878hg19UCSC Ensembl
Cytoband1p31.2
Allele length
AssemblyAllele length
hg381320
hg191320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17526091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6049004
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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