A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3752904



Internal ID19051185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15265119..15334474hg38UCSC Ensembl
Innerchr7:15304744..15374099hg19UCSC Ensembl
Innerchr7:15271269..15340624hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3869356
hg1969356
hg1869356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028108
Supporting Variants
Samples
Known GenesAGMO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3752904
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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