A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027389



Internal ID18769921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143773034..143881082hg38UCSC Ensembl
Innerchr7:143470127..143578175hg19UCSC Ensembl
Innerchr7:143101060..143209108hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38108049
hg19108049
hg18108049
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6718n100
Supporting Variantsnssv3671095
Samples
Known GenesFAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027389
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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