A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150499



Internal ID21512212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44746201..44746201hg38UCSC Ensembl
chr7:44785800..44785800hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625087
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150499
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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