A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3904604



Internal ID11857267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14591264..14592047hg38UCSC Ensembl
chrY:16703144..16703927hg19UCSC Ensembl
chrY:15212538..15213321hg18UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38784
hg19784
hg18784
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1500453
Supporting Variants
SamplesHuRef
Known GenesNLGN4Y
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3904604
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer