A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1070180



Internal ID18974034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73059461..73060362hg38UCSC Ensembl
chr13:73633599..73634500hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768722
SamplesKWP1
Known GenesKLF5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1070180
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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