A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937555



Internal ID21357625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130734056..130734056hg38UCSC Ensembl
chr7:130418883..130418883hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203972
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937555
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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