A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945758



Internal ID21365827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165708137..165708137hg38UCSC Ensembl
chr1:165677374..165677374hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15187529
SamplesHG002
Known GenesLOC440700
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945758
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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