A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959823



Internal ID18859151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:6240159..6266359hg38UCSC Ensembl
OuterchrY:6108200..6134400hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3826201
hg1926201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1119383
Supporting Variants
SamplesKWS1
Known GenesTSPY2, TTTY23, TTTY23B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959823
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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