A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427113



Internal ID22484983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136697601..136697601hg38UCSC Ensembl
chr6:137018739..137018739hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957024
Supporting Variants
Samples
Known GenesMAP3K5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427113
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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