A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999657



Internal ID19159193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44004296..44028601hg38UCSC Ensembl
Innerchr2:44231435..44255740hg19UCSC Ensembl
Innerchr2:44084939..44109244hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3824306
hg1924306
hg1824306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581585
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)nsv999657
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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