A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655157



Internal ID18953438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:83560572..83756449hg38UCSC Ensembl
Innerchr7:83189888..83385765hg19UCSC Ensembl
Innerchr7:83027824..83223701hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38195878
hg19195878
hg18195878
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017248
Supporting Variants
Samples
Known GenesMIR7976, SEMA3E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655157
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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