A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997444



Internal ID19156980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75434082..75537642hg38UCSC Ensembl
Innerchr3:75483233..75586793hg19UCSC Ensembl
Innerchr3:75565923..75669483hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38103561
hg19103561
hg18103561
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3596155, nssv3596154, nssv3733711
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997444
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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