A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006441



Internal ID19095658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:149501038..149544678hg38UCSC Ensembl
Innerchr2:150357552..150401192hg19UCSC Ensembl
Innerchr2:150065798..150109438hg18UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg3843641
hg1943641
hg1843641
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4093n100
Supporting Variantsnssv3582957
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)nsv1006441
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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