A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527155



Internal ID15454448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111203739..111472797hg38UCSC Ensembl
Innerchr7:110843795..111112853hg19UCSC Ensembl
Innerchr7:110631031..110900089hg18UCSC Ensembl
Innerchr7:110437746..110706804hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38269059
hg19269059
hg18269059
hg17269059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv427n21
Supporting Variantsnssv703546
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527155
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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