A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062804



Internal ID19152023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33306183..33352174hg38UCSC Ensembl
Innerchr17:31633201..31679192hg19UCSC Ensembl
Innerchr17:28657314..28703305hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3845992
hg1945992
hg1845992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3139n100
Supporting Variantsnssv3561057
Samples
Known GenesASIC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062804
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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