A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15198349



Internal ID21337145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55237642..55237707hg38UCSC Ensembl
chr7:55305335..55305400hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3925482
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15198349
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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