A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070405



Internal ID21490438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33907177..33907277hg38UCSC Ensembl
chr10:34196105..34196205hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591082
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070405
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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