A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960811



Internal ID18862939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:10978049..10978251hg38UCSC Ensembl
Outerchr1:11038106..11038308hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120069
Supporting Variants
SamplesKWS1
Known GenesC1orf127
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960811
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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