A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769696



Internal ID19305420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11599..72400hg38UCSC Ensembl
chr1:11599..72400hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3860802
hg1960802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076307
Supporting Variants
SamplesKWP1
Known GenesDDX11L1, FAM138A, FAM138F, MIR6859-1, MIR6859-2, OR4F5, WASH7P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769696
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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