A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017640



Internal ID18760174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:77643042..77681947hg38UCSC Ensembl
Innerchr7:77272359..77311264hg19UCSC Ensembl
Innerchr7:77110295..77149200hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3838906
hg1938906
hg1838906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6510n100
Supporting Variantsnssv3657116
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)nsv1017640
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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