A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003836



Internal ID18846941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9453790..9536991hg38UCSC Ensembl
OuterchrY:9291399..9374600hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3883202
hg1983202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151272
Supporting Variants
SamplesKWB1
Known GenesFAM197Y2, FAM197Y5, TSPY1, TSPY10, TSPY3, TSPY4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003836
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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