A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115925



Internal ID18911186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9333591..9403591hg38UCSC Ensembl
OuterchrY:9171200..9241200hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3870001
hg1970001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978487, nssv3987599
SamplesKWS2, KWS1
Known GenesFAM197Y2, FAM197Y5, TSPY10, TSPY3, TSPY4, TSPY8, TTTY20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115925
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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