A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600697



Internal ID21549338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4881150..4881225hg38UCSC Ensembl
chr10:4923342..4923417hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070610
SamplesHG00512
Known GenesAKR1C6P
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600697
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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