A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5637205



Internal ID21585510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6795262..6795262hg38UCSC Ensembl
chr10:6837224..6837224hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071276
SamplesNA19238
Known GenesLINC00707
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5637205
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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