A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766779



Internal ID18959056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1774848..1775021hg38UCSC Ensembl
chr12:1884014..1884187hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071001
Supporting Variants
SamplesKWP1
Known GenesADIPOR2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766779
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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