A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695014



Internal ID15084980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88579150..88591149hg38UCSC Ensembl
Innerchr7:88208465..88220464hg19UCSC Ensembl
Innerchr7:88046401..88058400hg18UCSC Ensembl
Innerchr7:87853116..87865115hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3812000
hg1912000
hg1812000
hg1712000
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515995
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695014
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