A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655208



Internal ID18606803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88889352..88918132hg38UCSC Ensembl
Innerchr7:88518666..88547446hg19UCSC Ensembl
Innerchr7:88356602..88385382hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3828781
hg1928781
hg1828781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028588
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)nssv3655208
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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