A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771354



Internal ID18966124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9453890..9536991hg38UCSC Ensembl
chrY:9291499..9374600hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3883102
hg1983102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077608
Supporting Variants
SamplesKWP1
Known GenesFAM197Y2, FAM197Y5, TSPY1, TSPY10, TSPY3, TSPY4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771354
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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