A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4234851



Internal ID11170703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150824285..150824480hg38UCSC Ensembl
chrX:149992758..149992953hg19UCSC Ensembl
chrX:149743416..149743611hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38196
hg19196
hg18196
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1216901
Supporting Variants
SamplesHuRef
Known GenesCD99L2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4234851
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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