A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151717



Internal ID21510958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168290660..168290714hg38UCSC Ensembl
chr6:168691340..168691394hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5567499
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151717
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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