A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466283



Internal ID21123836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43710265..43953275hg38UCSC Ensembl
chr11:43731815..43974825hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38243011
hg19243011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991369
Samples
Known GenesALKBH3, ALKBH3-AS1, C11orf96, HSD17B12, SEC14L1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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