A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143864



Internal ID18918248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:77958318..77959618hg38UCSC Ensembl
Outerchr17:75954400..75955700hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994561
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143864
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