A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764947



Internal ID18962296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66986680..66987090hg38UCSC Ensembl
chr1:67452363..67452773hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38411
hg19411
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078294
Supporting Variants
SamplesKWP1
Known GenesMIER1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764947
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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