A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055797



Internal ID19145016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:33313412..33350142hg38UCSC Ensembl
Innerchr17:31640430..31677160hg19UCSC Ensembl
Innerchr17:28664543..28701273hg18UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3836731
hg1936731
hg1836731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3139n100
Supporting Variantsnssv3561058
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)nsv1055797
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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