A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953732



Internal ID17302606
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 StatusM
Merged Variants
Supporting Variantsnssv3000345
SamplesBILGI_BIOE
Known GenesFAM197Y2, FAM197Y5, TSPY4, TSPY8
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953732
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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