A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155499



Internal ID22086004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81049653..81051263hg38UCSC Ensembl
Outerchr17:81047415..81055216hg38UCSC Ensembl
Innerchr17:79023453..79025063hg19UCSC Ensembl
Outerchr17:79021215..79029016hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg387802
hg197802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011881
Samples
Known GenesBAIAP2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155499
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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