A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772970



Internal ID19310111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168538964..168539276hg38UCSC Ensembl
chr2:169395474..169395786hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072042
Supporting Variants
SamplesKWP1
Known GenesCERS6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772970
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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