A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148878



Internal ID18853673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:10171690..10190791hg38UCSC Ensembl
OuterchrY:10009299..10028400hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3819102
hg1919102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997666
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148878
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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