A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4086864



Internal ID11328325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17502507..17502822hg38UCSC Ensembl
chrX:17520630..17520945hg19UCSC Ensembl
chrX:17430551..17430866hg18UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38316
hg19316
hg18316
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1528723
Supporting Variants
SamplesHuRef
Known GenesNHS
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4086864
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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