A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151016



Internal ID21460788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:18662370..18662370hg38UCSC Ensembl
chr7:18701993..18701993hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625037
Supporting Variants
SamplesHG02818
Known GenesHDAC9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151016
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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