A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5625283



Internal ID21573588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38359569..38359569hg38UCSC Ensembl
chr7:38399170..38399170hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17142680
SamplesHG02587
Known GenesTRG-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5625283
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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