A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655075



Internal ID18953356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6814467..6880637hg38UCSC Ensembl
Innerchr7:6854098..6920268hg19UCSC Ensembl
Innerchr7:6820623..6886793hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3866171
hg1966171
hg1866171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019159
Supporting Variants
Samples
Known GenesCCZ1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655075
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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