A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132077



Internal ID18935695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112502365..112502457hg38UCSC Ensembl
Outerchr9:115264645..115264737hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4127n106
Supporting Variantsnssv3986741
SamplesKWS1
Known GenesKIAA1958
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132077
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