A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017097



Internal ID18759632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37233136..37367949hg38UCSC Ensembl
Innerchr7:37272741..37407552hg19UCSC Ensembl
Innerchr7:37239266..37374077hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38134814
hg19134812
hg18134812
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643426
Samples
Known GenesELMO1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017097
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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