A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17156458



Internal ID21487921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136705494..136705494hg38UCSC Ensembl
chr6:137026632..137026632hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382761
hg192761
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625780
Supporting Variants
SamplesNA18534
Known GenesMAP3K5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17156458
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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