A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028400



Internal ID19117618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143728285..143816712hg38UCSC Ensembl
Innerchr7:143425378..143513805hg19UCSC Ensembl
Innerchr7:143056311..143144738hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3888428
hg1988428
hg1888428
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6709n100
Supporting Variantsnssv3670417
Samples
Known GenesCTAGE6, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028400
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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