A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525934



Internal ID15453227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:98223872..98236979hg38UCSC Ensembl
Innerchr7:97853184..97866291hg19UCSC Ensembl
Innerchr7:97691120..97704227hg18UCSC Ensembl
Innerchr7:97497835..97510942hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3813108
hg1913108
hg1813108
hg1713108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702140
Samples
Known GenesTECPR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525934
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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