A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621077



Internal ID21569382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216261661..216261661hg38UCSC Ensembl
chr2:217126384..217126384hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17110067
SamplesHG02587
Known GenesMARCH4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621077
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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