A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987371



Internal ID19211791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:33835578..33844078hg38UCSC Ensembl
Outerchr4:33837200..33845700hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg388501
hg198501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132587
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987371
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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