A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969972



Internal ID19230338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:78206587..78206639hg38UCSC Ensembl
Outerchr17:76202668..76202720hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113891
Supporting Variants
SamplesKWS2
Known GenesAFMID
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969972
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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