A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757552



Internal ID20533412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37179267..37179267hg38UCSC Ensembl
chr6:37147043..37147043hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273403
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757552
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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