A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953735



Internal ID16955922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9453792..9506291hg38UCSC Ensembl
OuterchrY:9291401..9343900hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3852500
hg1952500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000348
SamplesBILGI_BIOE
Known GenesFAM197Y2, FAM197Y5, TSPY1, TSPY4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953735
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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