A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767804



Internal ID19313597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63912123..63913224hg38UCSC Ensembl
chr3:63897799..63898900hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072697
Supporting Variants
SamplesKWP1
Known GenesATXN7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767804
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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