A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004178



Internal ID19093395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75372007..75500555hg38UCSC Ensembl
Innerchr3:75421158..75549706hg19UCSC Ensembl
Innerchr3:75503848..75632396hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38128549
hg19128549
hg18128549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3732997, nssv3732996
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)nsv1004178
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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