A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028756



Internal ID18771287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143773034..143870954hg38UCSC Ensembl
Innerchr7:143470127..143568047hg19UCSC Ensembl
Innerchr7:143101060..143198980hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3897921
hg1997921
hg1897921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6718n100
Supporting Variantsnssv3671092, nssv3671091
Samples
Known GenesFAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028756
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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