A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6481621



Internal ID9126954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44520621..44522150hg38UCSC Ensembl
OuterchrX:44520584..44522200hg38UCSC Ensembl
InnerchrX:44379867..44381396hg19UCSC Ensembl
OuterchrX:44379830..44381446hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381617
hg191617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669870
Supporting Variants
SamplesHG01149
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6481621
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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