A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032336



Internal ID19121558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124950634..125033319hg38UCSC Ensembl
Innerchr7:124590688..124673373hg19UCSC Ensembl
Innerchr7:124377924..124460609hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3882686
hg1982686
hg1882686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6607n100
Supporting Variantsnssv3662141
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)nsv1032336
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