A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3962770



Internal ID19220619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:51953842..52100894hg38UCSC Ensembl
Outerchr5:51249676..51396728hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38147053
hg19147053
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129337
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3962770
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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