A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145788



Internal ID21505450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75372681..75372731hg38UCSC Ensembl
chr6:76082397..76082447hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5584296
Supporting Variants
SamplesNA19650
Known GenesFILIP1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145788
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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