A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5897915



Internal ID22673025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124344200..124351991hg38UCSC Ensembl
chr6:124665346..124673137hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg387792
hg197792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428035
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5897915
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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