A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767546



Internal ID18961626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29420494..29420817hg38UCSC Ensembl
chr12:29573427..29573750hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070519
Supporting Variants
SamplesKWP1
Known GenesOVCH1-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767546
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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