A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149597



Internal ID18853502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9333390..9403591hg38UCSC Ensembl
OuterchrY:9170999..9241200hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3870202
hg1970202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000900
SamplesKWB1
Known GenesFAM197Y2, FAM197Y5, TSPY10, TSPY3, TSPY4, TSPY8, TTTY20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149597
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