A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058836



Internal ID19148055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13923515..14017889hg38UCSC Ensembl
Innerchr17:13826832..13921206hg19UCSC Ensembl
Innerchr17:13767557..13861931hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3894375
hg1994375
hg1894375
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560360
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058836
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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