A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1117674



Internal ID19270813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:151517556..151517635hg38UCSC Ensembl
Outerchr6:151838691..151838770hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3957780
SamplesKWS1
Known GenesCCDC170
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1117674
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