A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3674689



Internal ID18972970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155263004..155282191hg38UCSC Ensembl
Innerchr7:155054714..155073901hg19UCSC Ensembl
Innerchr7:154685647..154704834hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3819188
hg1919188
hg1819188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1024528
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)nssv3674689
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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