A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6010611



Internal ID9373340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195412946..195423700hg38UCSC Ensembl
chr3:195133675..195144429hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3810755
hg1910755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657233
Supporting Variants
SamplesNA18565
Known GenesACAP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6010611
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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