A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005041



Internal ID19094258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148773056..148934526hg38UCSC Ensembl
Innerchr1:144949963..145115473hg19UCSC Ensembl
Innerchr1:143661320..143826830hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38161471
hg19165511
hg18165511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv324n100
Supporting Variantsnssv3489848
Samples
Known GenesLOC100288142, NBPF12, NBPF9, PDE4DIP, SEC22B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005041
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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