A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947759



Internal ID22723261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150337841..150337841hg38UCSC Ensembl
chr6:150658977..150658977hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428613
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947759
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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