A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15181830



Internal ID21320626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63319320..63319374hg38UCSC Ensembl
chr11:63086792..63086846hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3934436
Supporting Variants
SamplesHG002
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15181830
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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