A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007840



Internal ID19097059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72275051..72345243hg38UCSC Ensembl
Innerchr1:72740734..72810926hg19UCSC Ensembl
Innerchr1:72513322..72583514hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3870193
hg1970193
hg1870193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv181n100
Supporting Variantsnssv3476071
Samples
Known GenesNEGR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007840
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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