A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655577



Internal ID18953858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65202834..65622681hg38UCSC Ensembl
Innerchr7:64663212..65087594hg19UCSC Ensembl
Innerchr7:64300647..64725029hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38419848
hg19424383
hg18424383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019070
Supporting Variants
Samples
Known GenesZNF92
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655577
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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