A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155896



Internal ID21408276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97420336..97420336hg38UCSC Ensembl
chr7:97049648..97049648hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg385988
hg195988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630264
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155896
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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