A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3977481



Internal ID19240761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:61360682..61372682hg38UCSC Ensembl
Outerchr4:62226400..62238400hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3812001
hg1912001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115672
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3977481
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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