A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072816



Internal ID18971386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7305336..7305635hg38UCSC Ensembl
chr3:7347023..7347322hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766695
SamplesKWP1
Known GenesGRM7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072816
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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