A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3939178



Internal ID21359247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68261430..68261430hg38UCSC Ensembl
chr4:69127148..69127148hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200470
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3939178
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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