A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5572037



Internal ID21520421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11313405..11313559hg38UCSC Ensembl
chr6:11313638..11313792hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159266
SamplesHG00171
Known GenesNEDD9
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5572037
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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