A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033270



Internal ID19122492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:101327634..101483000hg38UCSC Ensembl
Innerchr7:100970915..101126281hg19UCSC Ensembl
Innerchr7:100757635..100913001hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38155367
hg19155367
hg18155367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n100
Supporting Variantsnssv3656091, nssv3656092
Samples
Known GenesCOL26A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033270
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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