A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6072066



Internal ID9667870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122646306..122653682hg38UCSC Ensembl
chrX:121780159..121787535hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg387377
hg197377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673692
Supporting Variants
SamplesNA19397
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6072066
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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