A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988775



Internal ID19230423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:164925547..164925639hg38UCSC Ensembl
Outerchr6:165339036..165339128hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135221
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988775
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