A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011309



Internal ID19100526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:17980692..18018882hg38UCSC Ensembl
Innerchr2:18161958..18200148hg19UCSC Ensembl
Innerchr2:18025439..18063629hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3838191
hg1938191
hg1838191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3733n100
Supporting Variantsnssv3578932
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)nsv1011309
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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