A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063768



Internal ID18806299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69272201..69314995hg38UCSC Ensembl
Innerchr17:67268342..67311136hg19UCSC Ensembl
Innerchr17:64779937..64822731hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3842795
hg1942795
hg1842795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567761
Samples
Known GenesABCA5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063768
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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