A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15190844



Internal ID21329703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36287072..36287072hg38UCSC Ensembl
chr11:36308622..36308622hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38864
hg19864
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3948275
Supporting Variants
SamplesHG002
Known GenesCOMMD9
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15190844
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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