A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637947



Internal ID21586252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137300977..137300977hg38UCSC Ensembl
chr7:136985724..136985724hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38563
hg19563
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17155022
SamplesHG03009
Known GenesPTN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637947
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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