A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028665



Internal ID18771196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76336044..76445651hg38UCSC Ensembl
Innerchr7:75965361..76074968hg19UCSC Ensembl
Innerchr7:75803297..75912904hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38109608
hg19109608
hg18109608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656495
Samples
Known GenesSRCRB4D, YWHAG, ZP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028665
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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