A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15192644



Internal ID21331525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7071557..7071557hg38UCSC Ensembl
chr11:7092788..7092788hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38342
hg19342
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3931080
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15192644
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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