A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643256



Internal ID21591561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:88992136..88992136hg38UCSC Ensembl
chr6:89701855..89701855hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151259
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643256
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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