A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032637



Internal ID19121859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38793027..38863123hg38UCSC Ensembl
Innerchr7:38832627..38902723hg19UCSC Ensembl
Innerchr7:38799152..38869248hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3870097
hg1970097
hg1870097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643866
Samples
Known GenesVPS41
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032637
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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