A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001266



Internal ID19090483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:221675776..221736731hg38UCSC Ensembl
Innerchr2:222540496..222601451hg19UCSC Ensembl
Innerchr2:222248740..222309695hg18UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg3860956
hg1960956
hg1860956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3729359
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)nsv1001266
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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