A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576171



Internal ID16363580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81078215..81079015hg38UCSC Ensembl
Innerchr17:79052015..79052815hg19UCSC Ensembl
Innerchr17:76666610..76667410hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38801
hg19801
hg18801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877108
Samples
Known GenesBAIAP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576171
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer