A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3662094



Internal ID18960375
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 StatusS
Merged Variantsnsv1023232
Supporting Variants
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)nssv3662094
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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