A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3593162



Internal ID6633442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161620658..161886244hg38UCSC Ensembl
chr2:162477168..162742754hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38265587
hg19265587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10740658
SamplesHG03455
Known GenesSLC4A10
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3593162
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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