A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623868



Internal ID21572173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:177297944..177297944hg38UCSC Ensembl
chr2:178162672..178162672hg19UCSC Ensembl
Cytoband2q31.2
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17109893, nssv17109894
SamplesHG02587, NA19238
Known GenesLOC100130691
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623868
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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