A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152570



Internal ID21487199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139908430..139908430hg38UCSC Ensembl
chr6:140229567..140229567hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633929
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152570
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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