A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032484



Internal ID19121706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111271746..111713305hg38UCSC Ensembl
Innerchr7:110911802..111353361hg19UCSC Ensembl
Innerchr7:110699038..111140597hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38441560
hg19441560
hg18441560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645245
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032484
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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