A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031916



Internal ID19121138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111375478..111691496hg38UCSC Ensembl
Innerchr7:111015534..111331552hg19UCSC Ensembl
Innerchr7:110802770..111118788hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38316019
hg19316019
hg18316019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6573n100
Supporting Variantsnssv3645273
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)nsv1031916
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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