A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960865



Internal ID18869047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:30203827..30203883hg38UCSC Ensembl
Outerchr17:28530845..28530901hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120113
Supporting Variants
SamplesKWS1
Known GenesSLC6A4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960865
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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