A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624564



Internal ID21572869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151611576..151611576hg38UCSC Ensembl
chr6:151932711..151932711hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144668
SamplesHG00171
Known GenesCCDC170
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624564
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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