A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063998



Internal ID18806529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81415451..81472280hg38UCSC Ensembl
Innerchr17:79389251..79439306hg19UCSC Ensembl
Innerchr17:77003846..77053901hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3856830
hg1950056
hg1850056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3294n100
Supporting Variantsnssv3567881
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)nsv1063998
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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