A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977300



Internal ID18896078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:15347443..15375843hg38UCSC Ensembl
Outerchr16:15441300..15469700hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3828401
hg1928401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115493
Supporting Variants
SamplesKWS2
Known GenesNPIPA5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977300
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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