A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596677



Internal ID21545286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29696948..29697123hg38UCSC Ensembl
chr10:29985877..29986052hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070333
SamplesHG03009
Known GenesSVIL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596677
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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