A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004737



Internal ID19093954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56654209..56682105hg38UCSC Ensembl
Innerchr4:57520375..57548271hg19UCSC Ensembl
Innerchr4:57215132..57243028hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3827897
hg1927897
hg1827897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3625289
Samples
Known GenesHOPX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004737
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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