A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155584



Internal ID21441567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67016239..67016239hg38UCSC Ensembl
chr7:66481226..66481226hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5639391
Supporting Variants
SamplesHG00732
Known GenesTYW1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155584
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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