A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655209



Internal ID18606804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88950439..88982308hg38UCSC Ensembl
Innerchr7:88579753..88611622hg19UCSC Ensembl
Innerchr7:88417689..88449558hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3831870
hg1931870
hg1831870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016918
Supporting Variants
Samples
Known GenesZNF804B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655209
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