A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3971153



Internal ID18877973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:76935843..76935907hg38UCSC Ensembl
Outerchr17:74931925..74931989hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123146
Supporting Variants
SamplesKWS1
Known GenesMGAT5B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3971153
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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