A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv908824



Internal ID6270751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73966862..74152366hg19UCSC Ensembl
Outerchr17:73959857..74162997hg19UCSC Ensembl
Innerchr17:71478457..71663961hg18UCSC Ensembl
Outerchr17:71471452..71674592hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1546956
SamplesMS17208
Known GenesACOX1, C17orf106-CDK3, CDK3, EVPL, EXOC7, FOXJ1, GALR2, LOC100507218, RNF157, SRP68, TEN1, ZACN
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv908824
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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