A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001687



Internal ID19090904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:695756..926869hg38UCSC Ensembl
Innerchr2:695756..922555hg19UCSC Ensembl
Innerchr2:685756..912555hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38231114
hg19226800
hg18226800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3700n100
Supporting Variantsnssv3571268
Samples
Known GenesLINC01115
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001687
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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