A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025697



Internal ID19114914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111142640..111261530hg38UCSC Ensembl
Innerchr7:110782696..110901586hg19UCSC Ensembl
Innerchr7:110569932..110688822hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38118891
hg19118891
hg18118891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6565n100
Supporting Variantsnssv3645226, nssv3645223, nssv3645229, nssv3645224, nssv3645225, nssv3645228, nssv3645227
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)nsv1025697
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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