A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996441



Internal ID20563481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93056448..93489647hg38UCSC Ensembl
chr11:92789614..93222813hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38433200
hg19433200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461646
Supporting Variants
Samples
Known GenesCCDC67, SLC36A4, SMCO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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