A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152338



Internal ID21443602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37012986..37012986hg38UCSC Ensembl
chr6:36980762..36980762hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5643594
Supporting Variants
SamplesHG00732
Known GenesFGD2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152338
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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