A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960902



Internal ID19209267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:173224730..173228289hg38UCSC Ensembl
Outerchr4:174145881..174149440hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg383560
hg193560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120145
Supporting Variants
SamplesKWS1
Known GenesGALNT7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960902
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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