A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631876



Internal ID21580181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73861965..73861965hg38UCSC Ensembl
chr7:73276295..73276295hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151343
SamplesNA12329
Known GenesWBSCR28
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631876
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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