A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028556



Internal ID18771087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16364990..16400399hg38UCSC Ensembl
Innerchr7:16404615..16440024hg19UCSC Ensembl
Innerchr7:16371140..16406549hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3835410
hg1935410
hg1835410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643200
Samples
Known GenesISPD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028556
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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