A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3949625



Internal ID21369694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44746201..44746201hg38UCSC Ensembl
chr7:44785800..44785800hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203338
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3949625
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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