A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625283



Internal ID18923564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:56076751..56189215hg38UCSC Ensembl
Innerchr4:56942917..57055381hg19UCSC Ensembl
Innerchr4:56637674..56750138hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38112465
hg19112465
hg18112465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1007114
Supporting Variants
Samples
Known GenesKIAA1211
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625283
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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