A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003996



Internal ID19186577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:26637952..26673053hg38UCSC Ensembl
OuterchrY:28784099..28819200hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3835102
hg1935102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151433
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003996
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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