A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3972128



Internal ID18882590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:76719932..76720018hg38UCSC Ensembl
Outerchr17:74716014..74716100hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1123145
Supporting Variants
SamplesKWS2
Known GenesJMJD6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3972128
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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