A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6306352



Internal ID9348948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10576551..10583990hg38UCSC Ensembl
chr1:10636608..10644047hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg387440
hg197440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665377
Supporting Variants
SamplesNA18545
Known GenesPEX14
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6306352
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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