A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762032



Internal ID18963330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58491572..58492773hg38UCSC Ensembl
chr3:58477299..58478500hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381202
hg191202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073225
Supporting Variants
SamplesKWP1
Known GenesKCTD6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762032
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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