A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600839



Internal ID21549482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63747984..63748118hg38UCSC Ensembl
chr17:61825344..61825478hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096256
SamplesNA19238
Known GenesCCDC47
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600839
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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