A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643279



Internal ID18941560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23080136..23101507hg38UCSC Ensembl
Innerchr7:23119755..23141126hg19UCSC Ensembl
Innerchr7:23086280..23107651hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3821372
hg1921372
hg1821372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025707
Supporting Variants
Samples
Known GenesKLHL7-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643279
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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