A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415379



Internal ID22473249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139726624..139726624hg38UCSC Ensembl
chr4:140647778..140647778hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5948698
Supporting Variants
Samples
Known GenesMAML3, MGST2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415379
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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