A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151747



Internal ID18849038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9024942..9032288hg38UCSC Ensembl
Outerchr17:8928259..8935605hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg387347
hg197347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998929
SamplesKWB1
Known GenesNTN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151747
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