A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469500



Internal ID22527390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6704867..6707870hg38UCSC Ensembl
chr11:6726098..6729101hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383004
hg193004
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5847576
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469500
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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