A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17994149



Internal ID20561189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7756148..7855558hg38UCSC Ensembl
chr11:7777695..7877105hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3899411
hg1999411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452461
Supporting Variants
Samples
Known GenesLOC283299, OR5E1P, OR5P2, OR5P3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17994149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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