A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978487



Internal ID18892309
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 StatusS
Merged Variantsnsv1115925
Supporting Variants
SamplesKWS2
Known GenesFAM197Y2, FAM197Y5, TSPY10, TSPY3, TSPY4, TSPY8, TTTY20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978487
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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