A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6466626



Internal ID9444029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132259957..132260038hg38UCSC Ensembl
chr12:132836496..132836588hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3882
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670347
Supporting Variants
SamplesHG00309
Known GenesGALNT9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6466626
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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