A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517356



Internal ID15444649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:113901406..113925428hg38UCSC Ensembl
Innerchr10:115661165..115685187hg19UCSC Ensembl
Innerchr10:115651155..115675177hg18UCSC Ensembl
Innerchr10:115651155..115675177hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3824023
hg1924023
hg1824023
hg1724023
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv690091, nssv705768, nssv702461, nssv651806, nssv702245, nssv701769, nssv667818, nssv695635, nssv674139, nssv669144
Samples
Known GenesNHLRC2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517356
Frequency
Sample Size2026
Observed Gain3
Observed Loss7
Observed Complex0
Frequencyn/a


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