A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001550



Internal ID19090767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:7340344..7391950hg38UCSC Ensembl
Innerchr1:7400404..7452010hg19UCSC Ensembl
Innerchr1:7322991..7374597hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3851607
hg1951607
hg1851607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3480881
Samples
Known GenesCAMTA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001550
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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