A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969579



Internal ID18899037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:135179662..135181962hg38UCSC Ensembl
Outerchr6:135500800..135503100hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122138
Supporting Variants
SamplesKWS2
Known GenesMYB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969579
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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