A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762027



Internal ID18960430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55445044..55445301hg38UCSC Ensembl
chr4:56311211..56311468hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073334
Supporting Variants
SamplesKWP1
Known GenesCLOCK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762027
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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