A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772183



Internal ID19306543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11085423..11260924hg38UCSC Ensembl
chrY:13241099..13416600hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg38175502
hg19175502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077612
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772183
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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