A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984680



Internal ID19205159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:68084797..68085897hg38UCSC Ensembl
Outerchr16:68118700..68119800hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126432
Supporting Variants
SamplesKWS1
Known GenesNFATC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984680
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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