A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029560



Internal ID19118779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40140307..40176283hg38UCSC Ensembl
Innerchr7:40179906..40215882hg19UCSC Ensembl
Innerchr7:40146431..40182407hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3835977
hg1935977
hg1835977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6338n100
Supporting Variantsnssv3752951, nssv3752952
Samples
Known GenesC7orf10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029560
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer