A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3963258



Internal ID18881566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:178832340..178833086hg38UCSC Ensembl
Outerchr3:178550128..178550874hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120816
Supporting Variants
SamplesKWS2
Known GenesKCNMB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3963258
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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