A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640610



Internal ID21588915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15149038..15149038hg38UCSC Ensembl
chr10:15191037..15191037hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38941
hg19941
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069221
SamplesNA20847
Known GenesNMT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640610
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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