A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170160



Internal ID21314221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76443274..77083484hg38UCSC Ensembl
Outerchr7:76426530..77091265hg38UCSC Ensembl
Innerchr7:76072591..76712801hg19UCSC Ensembl
Outerchr7:76055847..76720582hg19UCSC Ensembl
Innerchr7:75910527..76550737hg18UCSC Ensembl
Outerchr7:75893783..76558518hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38664736
hg19664736
hg18664736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245194, nssv14252298, nssv14249600, nssv14243727, nssv14250093, nssv14249841
SamplesNGO_28, NGO_39, NGO_20, NGO_49
Known GenesDTX2, DTX2P1-UPK3BP1-PMS2P11, FDPSP2, LOC100132832, LOC100133091, POMZP3, UPK3B, ZP3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170160
Frequency
Sample Size93
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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