A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060977



Internal ID19150196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12864086..12971179hg38UCSC Ensembl
Innerchr17:12767403..12874496hg19UCSC Ensembl
Innerchr17:12708128..12815221hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38107094
hg19107094
hg18107094
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560353
Samples
Known GenesARHGAP44
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060977
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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