A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4091402



Internal ID11670473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:77885068..77885522hg38UCSC Ensembl
chrX:77140565..77141019hg19UCSC Ensembl
chrX:77027221..77027675hg18UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38455
hg19455
hg18455
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1784785
Supporting Variants
SamplesHuRef
Known GenesMAGT1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4091402
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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