A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000383



Internal ID17293335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:15210321..15214720hg38UCSC Ensembl
OuterchrY:17322201..17326600hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953095
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000383
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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