A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10886653



Internal ID1572772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237401278..237406744hg38UCSC Ensembl
Innerchr2:237401278..237406744hg38UCSC Ensembl
Outerchr2:237401164..237406843hg38UCSC Ensembl
chr2:238309921..238315387hg19UCSC Ensembl
Innerchr2:238309921..238315387hg19UCSC Ensembl
Outerchr2:238309807..238315486hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg385467
hg195467
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3594742
Supporting Variants
SamplesHG01456
Known GenesCOL6A3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10886653
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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