A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992637



Internal ID18880305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:13342823..13365642hg38UCSC Ensembl
Outerchr1:13669200..13692100hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3822820
hg1922901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141130
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992637
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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