A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020630



Internal ID19109849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38345240..38375788hg38UCSC Ensembl
Innerchr7:38384841..38415389hg19UCSC Ensembl
Innerchr7:38351366..38381914hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3830549
hg1930549
hg1830549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6336n100
Supporting Variantsnssv3643860
Samples
Known GenesTRG-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020630
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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