A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097796



Internal ID21430126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67609495..67609644hg38UCSC Ensembl
chr15:67901833..67901982hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593800
Supporting Variants
SamplesHG00731
Known GenesMAP2K5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097796
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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