A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3947357



Internal ID21367426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139101478..139101478hg38UCSC Ensembl
chr7:138786224..138786224hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15203443
SamplesHG002
Known GenesZC3HAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3947357
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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