A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967846



Internal ID18888510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:57256139..57257339hg38UCSC Ensembl
Outerchr17:55333500..55334700hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133410
Supporting Variants
SamplesKWS2
Known GenesMSI2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967846
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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