A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976265



Internal ID19228941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:97878421..97878489hg38UCSC Ensembl
Outerchr9:100640703..100640771hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115212
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976265
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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