A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755354



Internal ID20531214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49701607..49701607hg38UCSC Ensembl
chr6:49669320..49669320hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282670
Samples
Known GenesCRISP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4755354
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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