A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149750



Internal ID19199167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrY:20066533..20094003hg38UCSC Ensembl
OuterchrY:22228419..22255889hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg3827471
hg1927471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001051
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149750
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer