A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683936



Internal ID21205795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75541947..75542038hg38UCSC Ensembl
chr11:75252992..75253083hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683936
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.546875


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