A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681872



Internal ID21203731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64270856..64270932hg38UCSC Ensembl
chr11:64038328..64038404hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791084
Supporting Variants
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681872
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.566667


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