A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768660



Internal ID19311493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:23535252..23560053hg38UCSC Ensembl
chrY:25681399..25706200hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3824802
hg1924802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078716
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768660
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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