A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1115926



Internal ID19270181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:9453891..9536991hg38UCSC Ensembl
OuterchrY:9291500..9374600hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3883101
hg1983101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978488, nssv3959824
SamplesKWS2, KWS1
Known GenesFAM197Y2, FAM197Y5, TSPY1, TSPY10, TSPY3, TSPY4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1115926
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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