A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976394



Internal ID19227658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:53097228..53102228hg38UCSC Ensembl
Outerchr1:53562900..53567900hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1115343
Supporting Variants
SamplesKWS2
Known GenesSLC1A7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3976394
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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