A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000349



Internal ID17293301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9507992..9511591hg38UCSC Ensembl
OuterchrY:9345601..9349200hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953736
Supporting Variants
SamplesBILGI_BIOE
Known GenesTSPY4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000349
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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