A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146282



Internal ID19201591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:3526597..3539677hg38UCSC Ensembl
OuterchrY:3394638..3407718hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3813081
hg1913081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999485
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146282
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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