A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112715



Internal ID18929623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:78359819..78360519hg38UCSC Ensembl
Outerchr17:76355900..76356600hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967203
SamplesKWS2
Known GenesSOCS3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112715
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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