A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4075882



Internal ID11685992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:46951443..46971306hg38UCSC Ensembl
chrX:46810804..46830688hg19UCSC Ensembl
chrX:46695748..46715632hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3819864
hg1919885
hg1819885
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1121377
Supporting Variants
SamplesHuRef
Known GenesJADE3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4075882
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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