A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057744



Internal ID18800275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81402199..81462332hg38UCSC Ensembl
Innerchr17:79375999..79429358hg19UCSC Ensembl
Innerchr17:76990594..77043953hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3860134
hg1953360
hg1853360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567871, nssv3567872, nssv3567870
Samples
Known GenesBAHCC1, MIR3186
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057744
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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