A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638644



Internal ID21586949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:46310737..46310737hg38UCSC Ensembl
chr7:46350335..46350335hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158617
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638644
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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