A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994085



Internal ID20561125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65040220..65093556hg38UCSC Ensembl
chr11:64807692..64861028hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3853337
hg1953337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458120
Supporting Variants
Samples
Known GenesARL2-SNX15, CDCA5, NAALADL1, SAC3D1, SNX15, TMEM262, ZFPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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