A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067660



Internal ID21490834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126200781..126200857hg38UCSC Ensembl
chr10:127889350..127889426hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584865
Supporting Variants
SamplesNA19238
Known GenesADAM12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067660
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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