A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999577



Internal ID19159114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88834106..88876695hg38UCSC Ensembl
Innerchr2:89133619..89176211hg19UCSC Ensembl
Innerchr2:88914734..88957326hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3842590
hg1942593
hg1842593
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3928n100
Supporting Variantsnssv3728991
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)nsv999577
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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