A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976279



Internal ID19230643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:120732429..120732489hg38UCSC Ensembl
Outerchr9:123494707..123494767hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115224
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976279
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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