A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772615



Internal ID18962129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20666939..20667640hg38UCSC Ensembl
chr2:20866699..20867400hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071981
Supporting Variants
SamplesKWP1
Known GenesGDF7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772615
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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