A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019736



Internal ID19108954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111509204..111679596hg38UCSC Ensembl
Innerchr7:111149260..111319652hg19UCSC Ensembl
Innerchr7:110936496..111106888hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38170393
hg19170393
hg18170393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6586n100
Supporting Variantsnssv3751507
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)nsv1019736
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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