A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891222



Internal ID18838932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143731945..143760627hg38UCSC Ensembl
Outerchr7:143719827..143784885hg38UCSC Ensembl
Innerchr7:143429038..143457720hg19UCSC Ensembl
Outerchr7:143416920..143481978hg19UCSC Ensembl
Innerchr7:143059971..143088653hg18UCSC Ensembl
Outerchr7:143047853..143112911hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3865059
hg1965059
hg1865059
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786024, essv25789074
Samples
Known GenesCTAGE6, FAM115C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891222
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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