A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027558



Internal ID19116777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126421217..126441119hg38UCSC Ensembl
Innerchr7:126061271..126081173hg19UCSC Ensembl
Innerchr7:125848507..125868409hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3819903
hg1919903
hg1819903
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662176
Samples
Known GenesGRM8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027558
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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