A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17070200



Internal ID21481574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38106141..38106141hg38UCSC Ensembl
chr10:38395069..38395069hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg383034
hg193034
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634029
Supporting Variants
SamplesHG03683
Known GenesZNF37A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17070200
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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