A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765007



Internal ID19315179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10132029..10142637hg38UCSC Ensembl
chrY:9969638..9980246hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3810609
hg1910609
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068325
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765007
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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