A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009528



Internal ID19098746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:178690798..178707719hg38UCSC Ensembl
Innerchr1:178659933..178676854hg19UCSC Ensembl
Innerchr1:176926556..176943477hg18UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3816922
hg1916922
hg1816922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv468n100
Supporting Variantsnssv3487287
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)nsv1009528
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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