A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072241



Internal ID19319827
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 StatusM
Merged Variants
Supporting Variantsnssv3771692
SamplesKWP1
Known GenesANKRD28
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072241
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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