A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024735



Internal ID19113952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40109628..40163757hg38UCSC Ensembl
Innerchr7:40149227..40203356hg19UCSC Ensembl
Innerchr7:40115752..40169881hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3854130
hg1954130
hg1854130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643872
Samples
Known GenesC7orf10, MPLKIP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024735
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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