A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691992



Internal ID15081958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143352880..143400007hg38UCSC Ensembl
Innerchr7:143049973..143097100hg19UCSC Ensembl
Innerchr7:142760095..142807222hg18UCSC Ensembl
Innerchr7:142566810..142613937hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3847128
hg1947128
hg1847128
hg1747128
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517520
Supporting Variants
Samples
Known GenesEPHA1, FAM131B, MIR6892, ZYX
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691992
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