A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3645216



Internal ID18596811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110616477..110733254hg38UCSC Ensembl
Innerchr7:110256533..110373310hg19UCSC Ensembl
Innerchr7:110043769..110160546hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38116778
hg19116778
hg18116778
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026955
Supporting Variants
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)nssv3645216
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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