A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003903



Internal ID19093121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:89910654..90026771hg38UCSC Ensembl
Innerchr4:90831805..90947922hg19UCSC Ensembl
Innerchr4:91050828..91166945hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38116118
hg19116118
hg18116118
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5336n100
Supporting Variantsnssv3633933
Samples
Known GenesMMRN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003903
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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