A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613108



Internal ID21561413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:965203..965203hg38UCSC Ensembl
chr2:960889..960889hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115316, nssv17115317
SamplesHG00731, HG00732
Known GenesSNTG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613108
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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