A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077773



Internal ID19320770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:868497..895815hg38UCSC Ensembl
chr17:771737..799055hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3827319
hg1927319
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763345
SamplesKWP1
Known GenesNXN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077773
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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