A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630837



Internal ID21579142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130884502..130884502hg38UCSC Ensembl
chr7:130569261..130569261hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140781
SamplesHG00096
Known GenesLOC646329
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630837
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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