A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4363178



Internal ID11299030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:150824190..150824281hg38UCSC Ensembl
chrX:149992663..149992754hg19UCSC Ensembl
chrX:149743321..149743412hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3892
hg1992
hg1892
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1531534
Supporting Variants
SamplesHuRef
Known GenesCD99L2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4363178
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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