A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1079030



Internal ID18972493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35822512..35970451hg38UCSC Ensembl
chr17:34149516..34297455hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38147940
hg19147940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770506
SamplesKWP1
Known GenesC17orf66, CCL5, LYZL6, RDM1, TAF15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1079030
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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