A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3561065



Internal ID18512660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33633605..34608994hg38UCSC Ensembl
Innerchr17:31960624..32936013hg19UCSC Ensembl
Innerchr17:28984737..29960126hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38975390
hg19975390
hg18975390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064104
Supporting Variants
Samples
Known GenesASIC2, C17orf102, CCL1, CCL11, CCL13, CCL2, CCL7, CCL8, TMEM132E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3561065
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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