A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4000858



Internal ID18843031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39107617..39115363hg38UCSC Ensembl
Outerchr9:65620499..65628200hg19UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg387747
hg197702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149553
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4000858
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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