A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674864



Internal ID9940969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24166203..24166827hg38UCSC Ensembl
OuterchrX:24166166..24166877hg38UCSC Ensembl
InnerchrX:24184320..24184944hg19UCSC Ensembl
OuterchrX:24184283..24184994hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38712
hg19712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6541782
SamplesNA19375
Known GenesZFX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674864
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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