A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023232



Internal ID19112449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119930209..119989882hg38UCSC Ensembl
Innerchr7:119570263..119629936hg19UCSC Ensembl
Innerchr7:119357499..119417172hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3859674
hg1959674
hg1859674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6601n100
Supporting Variantsnssv3662094
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023232
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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