A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3751528



Internal ID19049809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:122093318..122160326hg38UCSC Ensembl
Innerchr7:121733372..121800380hg19UCSC Ensembl
Innerchr7:121520608..121587616hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3867009
hg1967009
hg1867009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019004
Supporting Variants
Samples
Known GenesAASS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3751528
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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