A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001777



Internal ID19090994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:150495413..150539106hg38UCSC Ensembl
Innerchr2:151351927..151395620hg19UCSC Ensembl
Innerchr2:151060173..151103866hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg3843694
hg1943694
hg1843694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582962
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)nsv1001777
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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