A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953882



Internal ID16956069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:36182421..36224156hg38UCSC Ensembl
Outerchr17:34509801..34551600hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3841736
hg1941800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998728
SamplesBILGI_BIOE
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953882
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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