A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030379



Internal ID19119598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119932900..119995388hg38UCSC Ensembl
Innerchr7:119572954..119635442hg19UCSC Ensembl
Innerchr7:119360190..119422678hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3862489
hg1962489
hg1862489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6601n100
Supporting Variantsnssv3751524, nssv3662099, nssv3662102, nssv3662101, nssv3662098, nssv3662100
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030379
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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