A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110921



Internal ID18904050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:76728429..76751381hg38UCSC Ensembl
Outerchr17:74724511..74747463hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3822953
hg1922953
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961339
SamplesKWS1
Known GenesMETTL23, MFSD11, MIR636, SRSF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110921
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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