A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030577



Internal ID18773108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:21509291..21641761hg38UCSC Ensembl
Innerchr7:21548909..21681379hg19UCSC Ensembl
Innerchr7:21515434..21647904hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38132471
hg19132471
hg18132471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6305n100
Supporting Variantsnssv3643271
Samples
Known GenesDNAH11, SP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030577
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