A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17107796



Internal ID21494337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:101777347..101784975hg38UCSC Ensembl
chr2:102393809..102401437hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg387629
hg197629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5579048
Supporting Variants
SamplesNA19238
Known GenesMAP4K4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17107796
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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