A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019217



Internal ID19108435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64060367..64341728hg38UCSC Ensembl
Innerchr7:63520745..63802106hg19UCSC Ensembl
Innerchr7:63158180..63439541hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38281362
hg19281362
hg18281362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6434n100
Supporting Variantsnssv3661969
Samples
Known GenesZNF679, ZNF727, ZNF735, ZNF736
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019217
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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