A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575893



Internal ID16363302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66292519..66299570hg38UCSC Ensembl
Innerchr17:64288637..64295688hg19UCSC Ensembl
Innerchr17:61719099..61726150hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg387052
hg197052
hg187052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875839, nssv875841, nssv875843, nssv875838, nssv875842, nssv875845, nssv875847, nssv875844, nssv875840, nssv875846
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575893
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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