A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3951067



Internal ID21371136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150589727..150589727hg38UCSC Ensembl
chr6:150910863..150910863hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15202628
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3951067
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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