A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962778



Internal ID19218634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:39212001..39225517hg38UCSC Ensembl
Outerchr1:39677673..39691189hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3813517
hg1913517
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129344
Supporting Variants
SamplesKWS1
Known GenesMACF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962778
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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