A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078713



Internal ID19321418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21228413..21236214hg38UCSC Ensembl
chrY:23390299..23398100hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg387802
hg197802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3762005
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078713
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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