A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6480056



Internal ID9622494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:137424857..137429263hg38UCSC Ensembl
OuterchrX:137424486..137429633hg38UCSC Ensembl
InnerchrX:136507016..136511422hg19UCSC Ensembl
OuterchrX:136506645..136511792hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg385148
hg195148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661325
Supporting Variants
SamplesNA19332
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6480056
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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