A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004032



Internal ID18746563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:273074..312959hg38UCSC Ensembl
Innerchr4:266863..306748hg19UCSC Ensembl
Innerchr4:256863..296748hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3839886
hg1939886
hg1839886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616084
Samples
Known GenesZNF732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004032
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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