A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3768584



Internal ID19310020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53163037..53163843hg38UCSC Ensembl
chr5:52458867..52459673hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38807
hg19807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073457
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3768584
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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