A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078876



Internal ID18976994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75111859..75698607hg38UCSC Ensembl
chr1:75577544..76164292hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38586749
hg19586749
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771412
SamplesKWP1
Known GenesLHX8, SLC44A5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078876
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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