A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115942



Internal ID19281566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:23069953..23102653hg38UCSC Ensembl
OuterchrY:25216100..25248800hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3832701
hg1932701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978505
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115942
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer