A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6372995



Internal ID9170548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151911344..151920550hg38UCSC Ensembl
OuterchrX:151910973..151920920hg38UCSC Ensembl
InnerchrX:151079816..151089022hg19UCSC Ensembl
OuterchrX:151079445..151089392hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg389948
hg199948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656900
Supporting Variants
SamplesHG01375
Known GenesMAGEA4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6372995
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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