A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771692



Internal ID19315050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15803492..15805693hg38UCSC Ensembl
chr3:15844999..15847200hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg382202
hg192202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072241
Supporting Variants
SamplesKWP1
Known GenesANKRD28
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771692
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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