A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10730684



Internal ID732500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159183805..159201028hg38UCSC Ensembl
chr2:160040316..160057539hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3817224
hg1917224
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3593110
Supporting Variants
SamplesNA19355
Known GenesMIR6888, TANC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10730684
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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