A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6550860



Internal ID8873579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:169659228..169662934hg38UCSC Ensembl
Outerchr3:169658857..169663304hg38UCSC Ensembl
Innerchr3:169377016..169380722hg19UCSC Ensembl
Outerchr3:169376645..169381092hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg384448
hg194448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676634
Supporting Variants
SamplesHG00326
Known GenesMECOM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6550860
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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