A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109106



Internal ID18926823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:73412029..73412098hg38UCSC Ensembl
Outerchr17:71408168..71408237hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954952
SamplesKWS1
Known GenesSDK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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