A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077607



Internal ID18978908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9333590..9403391hg38UCSC Ensembl
chrY:9171199..9241000hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3869802
hg1969802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771333
SamplesKWP1
Known GenesFAM197Y2, FAM197Y5, TSPY10, TSPY3, TSPY4, TSPY8, TTTY20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077607
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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