A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6149172



Internal ID9126575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92319545..92322987hg38UCSC Ensembl
chr10:94079302..94082744hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg383443
hg193443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670111
Supporting Variants
SamplesNA19451
Known GenesMARCH5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6149172
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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