A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1076892



Internal ID18971314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50303703..50304504hg38UCSC Ensembl
chr7:50343299..50344100hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg38802
hg19802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764350
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1076892
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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