A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023334



Internal ID18765867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110603539..110749639hg38UCSC Ensembl
Innerchr7:110243595..110389695hg19UCSC Ensembl
Innerchr7:110030831..110176931hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38146101
hg19146101
hg18146101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6564n100
Supporting Variantsnssv3751484
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)nsv1023334
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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