A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078718



Internal ID19321336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26088652..26126853hg38UCSC Ensembl
chrY:28234799..28273000hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg3838202
hg1938202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768264
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078718
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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