A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677663



Internal ID9943768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1607754..1613590hg38UCSC Ensembl
OuterchrX:1607717..1613640hg38UCSC Ensembl
InnerchrX:1726647..1732483hg19UCSC Ensembl
OuterchrX:1726610..1732533hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg385924
hg195924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6440402
SamplesHG01375
Known GenesASMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677663
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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