A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767556



Internal ID19313096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:281532..314233hg38UCSC Ensembl
chrY:148199..180900hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3832702
hg1932702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077604
Supporting Variants
SamplesKWP1
Known GenesGTPBP6, PLCXD1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767556
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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