A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915582



Internal ID22690800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61149797..61168615hg38UCSC Ensembl
chr11:60917269..60936087hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3818819
hg1918819
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355945
Samples
Known GenesVPS37C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915582
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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