A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987906



Internal ID19217539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:78358363..78359687hg38UCSC Ensembl
Outerchr5:77654187..77655511hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381325
hg191325
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133094
Supporting Variants
SamplesKWS1
Known GenesLOC728769
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987906
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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