A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3633934



Internal ID18932215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:89933404..90031572hg38UCSC Ensembl
Innerchr4:90854555..90952723hg19UCSC Ensembl
Innerchr4:91073578..91171746hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3898169
hg1998169
hg1898169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998230
Supporting Variants
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)nssv3633934
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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