A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667783



Internal ID9587202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:1406650..1407191hg38UCSC Ensembl
OuterchrX:1406613..1407241hg38UCSC Ensembl
InnerchrX:1525543..1526084hg19UCSC Ensembl
OuterchrX:1525506..1526134hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5908869
SamplesNA19818
Known GenesASMTL, ASMTL-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667783
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer