A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961339



Internal ID18871216
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 StatusS
Merged Variantsnsv1110921
Supporting Variants
SamplesKWS1
Known GenesMETTL23, MFSD11, MIR636, SRSF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961339
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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