A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146714



Internal ID19200436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:26284852..26303753hg38UCSC Ensembl
OuterchrY:28430999..28449900hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3818902
hg1918902
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995869
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146714
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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