A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678334



Internal ID9597753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7342138..7342381hg38UCSC Ensembl
chrX:7260179..7260422hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38244
hg19244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6543352, essv5709713, essv6325379
SamplesHG01079, HG01204, HG01061
Known GenesSTS
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678334
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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