A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133707



Internal ID19257797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:39445501..39481701hg38UCSC Ensembl
Outerchr9:39443500..39481700hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3836201
hg1938201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969280
SamplesKWS2
Known GenesLOC653501, ZNF658B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133707
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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