A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6033899



Internal ID9468035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3195159..3195720hg38UCSC Ensembl
chr6:3195393..3195954hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38562
hg19562
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663370
Supporting Variants
SamplesNA18934
Known GenesLOC100507194
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6033899
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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