A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141877



Internal ID21511938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155782148..155782148hg38UCSC Ensembl
chr7:155574842..155574842hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5628942
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141877
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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