A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771946



Internal ID19309568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:24179252..24194453hg38UCSC Ensembl
chrY:26325399..26340600hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3815202
hg1915202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076749
Supporting Variants
SamplesKWP1
Known GenesCSPG4P1Y
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771946
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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