A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643877



Internal ID18595472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40297510..40388035hg38UCSC Ensembl
Innerchr7:40337109..40427634hg19UCSC Ensembl
Innerchr7:40303634..40394159hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3890526
hg1990526
hg1890526
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017909
Supporting Variants
Samples
Known GenesC7orf10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643877
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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