A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055358



Internal ID19144577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14709678..15055196hg38UCSC Ensembl
Innerchr17:14612995..14958513hg19UCSC Ensembl
Innerchr17:14553720..14899238hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38345519
hg19345519
hg18345519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560380
Samples
Known GenesCDRT7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055358
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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