A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5640072



Internal ID21588377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34665840..34665840hg38UCSC Ensembl
chr10:34954768..34954768hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070168, nssv17070167
SamplesHG03486, NA19238
Known GenesPARD3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5640072
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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