A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633266



Internal ID6673388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96217016..96229240hg38UCSC Ensembl
Innerchr13:96217026..96229230hg38UCSC Ensembl
Outerchr13:96217006..96229250hg38UCSC Ensembl
chr13:96869270..96881494hg19UCSC Ensembl
Innerchr13:96869280..96881484hg19UCSC Ensembl
Outerchr13:96869260..96881504hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3812225
hg1912225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14869278
SamplesHG02407
Known GenesHS6ST3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633266
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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