A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657975



Internal ID21606280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41031545..41031545hg38UCSC Ensembl
chr15:41323743..41323743hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085844, nssv17090996
SamplesHG00731, HG00732
Known GenesINO80
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657975
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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