A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3656677



Internal ID18608272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76568101..76940323hg38UCSC Ensembl
Innerchr7:76197418..76569640hg19UCSC Ensembl
Innerchr7:76035354..76407576hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38372223
hg19372223
hg18372223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022762
Supporting Variants
Samples
Known GenesLOC100133091, POMZP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3656677
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