A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020555



Internal ID18763090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143729961..143773176hg38UCSC Ensembl
Innerchr7:143427054..143470269hg19UCSC Ensembl
Innerchr7:143057987..143101202hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3843216
hg1943216
hg1843216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6708n100
Supporting Variantsnssv3670420
Samples
Known GenesCTAGE6, FAM115C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020555
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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