A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113871



Internal ID19279466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:40673234..40673302hg38UCSC Ensembl
Outerchr17:38829486..38829554hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3954557, nssv3972525
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113871
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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