A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10845292



Internal ID6478406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:215641388..215719779hg38UCSC Ensembl
chr2:216506111..216584502hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3878392
hg1978392
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3594277
Supporting Variants
SamplesNA20524
Known GenesLINC00607
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10845292
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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