A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658370



Internal ID9924475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62622502..62686731hg38UCSC Ensembl
OuterchrX:62622468..62686766hg38UCSC Ensembl
InnerchrX:61841972..61906201hg19UCSC Ensembl
OuterchrX:61841938..61906236hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3864299
hg1964299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6099888
SamplesHG00109
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658370
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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