A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6081898



Internal ID9059301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158844017..158853440hg38UCSC Ensembl
chr1:158813807..158823230hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg389424
hg199424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2669506
Supporting Variants
SamplesHG01125
Known GenesMNDA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6081898
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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