A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076289



Internal ID19316859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:328064..329665hg38UCSC Ensembl
chrY:238799..240400hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765870
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076289
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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