A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138560



Internal ID19282667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:58663250..58663315hg38UCSC Ensembl
Outerchr17:56740611..56740676hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991148
SamplesKWS2
Known GenesTEX14
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138560
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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