A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064572



Internal ID19153791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:56081095..56096102hg38UCSC Ensembl
Innerchr17:54158456..54173463hg19UCSC Ensembl
Innerchr17:51513455..51528462hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3815008
hg1915008
hg1815008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3267n100
Supporting Variantsnssv3724983, nssv3724982
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064572
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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