A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000345



Internal ID17293297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9337692..9375791hg38UCSC Ensembl
OuterchrY:9175301..9213400hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3838100
hg1938100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953732
Supporting Variants
SamplesBILGI_BIOE
Known GenesFAM197Y2, FAM197Y5, TSPY4, TSPY8
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000345
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