A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3967845



Internal ID18882576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:56593339..56593939hg38UCSC Ensembl
Outerchr17:54670700..54671300hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133409
Supporting Variants
SamplesKWS2
Known GenesNOG
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3967845
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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