A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702213



Internal ID15438865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62575192..62780663hg38UCSC Ensembl
Innerchr7:62035570..62241041hg19UCSC Ensembl
Innerchr7:61673005..61878476hg18UCSC Ensembl
Innerchr7:61479720..61685191hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38205472
hg19205472
hg18205472
hg17205472
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516283
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702213
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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