A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5919837



Internal ID9079940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100022662..100037900hg38UCSC Ensembl
Outerchr3:100022625..100037950hg38UCSC Ensembl
Innerchr3:99741506..99756744hg19UCSC Ensembl
Outerchr3:99741469..99756794hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3815326
hg1915326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2671411
Supporting Variants
SamplesHG01055
Known GenesCMSS1, FILIP1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5919837
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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