A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133590



Internal ID19257987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:182144347..182144947hg38UCSC Ensembl
Outerchr4:183065500..183066100hg19UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969154
SamplesKWS2
Known GenesMGC45800
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133590
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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