A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3621351



Internal ID11793831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17952227..18638948hg38UCSC Ensembl
chrY:20064107..20800834hg19UCSC Ensembl
chrY:18573501..19260222hg18UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg38686722
hg19736728
hg18686722
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1670141
Supporting Variants
SamplesHuRef
Known GenesCDY2A, CDY2B, FAM224A, FAM224B, FAM41AY1, FAM41AY2, HSFY1, HSFY2, TTTY9A, TTTY9B, XKRY, XKRY2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3621351
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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