A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771890



Internal ID19310580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195688121..195960519hg38UCSC Ensembl
chr3:195414992..195687390hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38272399
hg19272399
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068315
Supporting Variants
SamplesKWP1
Known GenesMIR570, MIR6829, MUC20, MUC4, SDHAP1, SDHAP2, TNK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771890
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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