A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968591



Internal ID19231024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:979060..979460hg38UCSC Ensembl
Outerchr17:882300..882700hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121925
Supporting Variants
SamplesKWS2
Known GenesNXN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968591
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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