A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070596



Internal ID19326223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76827664..76828365hg38UCSC Ensembl
chr13:77401799..77402500hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765370
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070596
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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