A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950159



Internal ID17299033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:34511424..34527223hg38UCSC Ensembl
Outerchr6:34479201..34495000hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3815800
hg1915800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997431
SamplesBILGI_BIOE
Known GenesPACSIN1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950159
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