A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3886481



Internal ID11875390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49115525..49115525hg38UCSC Ensembl
chrX:48971879..48971879hg19UCSC Ensembl
chrX:48858823..48858823hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38571
hg19571
hg18571
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1526582
Supporting Variants
SamplesHuRef
Known GenesGPKOW
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3886481
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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