A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995785



Internal ID19188656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:132421594..132421692hg38UCSC Ensembl
Outerchr9:135296981..135297079hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146630
Supporting Variants
SamplesKWB1
Known GenesC9orf171
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3995785
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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