A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141443



Internal ID21470751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156013075..156013075hg38UCSC Ensembl
chr7:155805769..155805769hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5626183
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141443
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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