A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768914



Internal ID18961979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16317770..16317834hg38UCSC Ensembl
chr3:16359277..16359341hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072242
Supporting Variants
SamplesKWP1
Known GenesRFTN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768914
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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