A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576170



Internal ID16363579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81078058..81078765hg38UCSC Ensembl
Innerchr17:79051858..79052565hg19UCSC Ensembl
Innerchr17:76666453..76667160hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38708
hg19708
hg18708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877107
Samples
Known GenesBAIAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576170
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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