A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638203



Internal ID21586508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83170913..83170913hg38UCSC Ensembl
chr7:82800229..82800229hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150643
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638203
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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