A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772377



Internal ID19312094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23776173..23798726hg38UCSC Ensembl
chr7:23815792..23838345hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3822554
hg1922554
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068712
Supporting Variants
SamplesKWP1
Known GenesSTK31
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772377
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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