A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967901



Internal ID18885568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:126326621..126327121hg38UCSC Ensembl
Outerchr9:129088900..129089400hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113015
Supporting Variants
SamplesKWS2
Known GenesMVB12B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967901
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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