A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148698



Internal ID21507323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136737041..136737041hg38UCSC Ensembl
chr6:137058179..137058179hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634127
Supporting Variants
SamplesNA19983
Known GenesMAP3K5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148698
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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