A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7837033



Internal ID14691632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155282327..155282328hg38UCSC Ensembl
InnerchrX:155282299..155282356hg38UCSC Ensembl
OuterchrX:155282298..155282357hg38UCSC Ensembl
chrX:154511616..154511617hg19UCSC Ensembl
InnerchrX:154511588..154511645hg19UCSC Ensembl
OuterchrX:154511587..154511646hg19UCSC Ensembl
chrX:154164810..154164811hg18UCSC Ensembl
InnerchrX:154164839..154164782hg18UCSC Ensembl
OuterchrX:154164781..154164840hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38175
hg19175
hg18175
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3308775
Supporting Variants
SamplesNA19239
Known GenesCLIC2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7837033
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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