A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628567



Internal ID21576872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7358074..7358074hg38UCSC Ensembl
chr10:7400036..7400036hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071397
SamplesNA19983
Known GenesSFMBT2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628567
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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