A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3929676



Internal ID21349745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15350308..15350308hg38UCSC Ensembl
chr4:15351932..15351932hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15190634
SamplesHG002
Known GenesC1QTNF7
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3929676
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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