A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668443



Internal ID15405095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111319825..111656173hg38UCSC Ensembl
Innerchr7:110959881..111296229hg19UCSC Ensembl
Innerchr7:110747117..111083465hg18UCSC Ensembl
Innerchr7:110553832..110890180hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38336349
hg19336349
hg18336349
hg17336349
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517394
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668443
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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