A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981526



Internal ID18270037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:73193985..73282738hg38UCSC Ensembl
Innerchr7:72608025..72696755hg19UCSC Ensembl
Innerchr7:72245961..72334691hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3888754
hg1988731
hg1888731
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2464970, nssv2464971, nssv2464966, nssv2464973, nssv2464968, nssv2464967, nssv2464972, nssv2464975, nssv2464974, nssv2464969
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGTF2IP1, LOC100093631, NCF1B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981526
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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