A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3762911



Internal ID18964949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:248574798..248634999hg38UCSC Ensembl
chr1:248738099..248798300hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3860202
hg1960202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068651
Supporting Variants
SamplesKWP1
Known GenesOR2T10, OR2T11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3762911
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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