A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656777



Internal ID21605082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:46155803..46155803hg38UCSC Ensembl
chr12:46549586..46549586hg19UCSC Ensembl
Cytoband12q13.11
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088564, nssv17088557, nssv17079739
SamplesHG00731, HG00732, NA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656777
Frequency
Sample Size35
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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