A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632756



Internal ID7019567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75900866..75977307hg38UCSC Ensembl
chr13:76475002..76551443hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3876442
hg1976442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv351e214
Supporting Variantsessv14800699, essv14800697, essv14800698
SamplesHG03578, HG03755, NA19438
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632756
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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