A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1670141



Internal ID12833259
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 StatusM
Merged Variants
Supporting Variantsessv3621351
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)esv1670141
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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